Process for the preparation of UV absorbers

Patent metadata

Field	Value
Publication number	US-12291509-B2
Application number	US-202017421326-A
Country	US
Kind code	B2
Filing date	Jan 2, 2020
Priority date	Jan 8, 2019
Publication date	May 6, 2025
Grant date	May 6, 2025

Abstract

The presently claimed invention relates to a novel, highly efficient and general process for the preparation of UV absorbers.

First claim

The invention claimed is:

1. A process for preparing a compound of formula (A)

wherein Ar 1 and Ar 2 are independently a moiety of the formula (B),

wherein
R 1 , R 2 , R 3 , R 4 and R 5 are independently selected from the group consisting of hydrogen, halogen, substituted or unsubstituted, linear or branched C 1 -C 24 alkyl, substituted or unsubstituted, linear or branched C 2 -C 24 alkenyl, substituted or unsubstituted C 5 -C 24 cycloalkyl, substituted or unsubstituted C 5 -C 24 cycloalkenyl, substituted or unsubstituted C 6 -C 24 aryl, substituted or unsubstituted C 7 -C 24 arylalkyl, C(═O)R, OR, NRR′, C(═O) NRR′, CN, SR, S(═O) 2 R, S(═O) 2 OH and S(═O) 2 OM; wherein M is an alkali metal; or
R 1 and R 2 together with the carbon atoms to which they are bonded or
R 2 and R 3 together with the carbon atoms to which they are bonded or
R 3 and R 4 together with the carbon atoms to which they are bonded or
R 4 and R 5 together with the carbon atoms to which they are bonded form an unsaturated or aromatic 5- to 20-membered carbocyclic ring that optionally contains 1, 2 or 3 heteroatom(s) selected from O, N or S as ring member(s);
Q is selected from hydrogen and OH;
R 6 is selected from the group consisting of hydrogen, substituted or unsubstituted, linear or branched C 1 -C 24 alkyl, substituted or unsubstituted, linear or branched C 2 -C 24 alkenyl, substituted or unsubstituted C 6 -C 24 aryl, substituted or unsubstituted C 7 -C 24 arylalkyl, substituted or unsubstituted C 5 -C 24 cycloalkyl and substituted or unsubstituted C 5 -C 24 cycloalkenyl, and C(═O)R;
R 7 , R 8 and R 9 are independently selected from the group consisting of hydrogen, halogen, substituted or unsubstituted, linear or branched C 1 -C 24 alkyl, substituted or unsubstituted, linear or branched C 2 -C 24 alkenyl, substituted or unsubstituted C 6 -C 24 aryl, substituted or unsubstituted C 7 -C 24 arylalkyl, substituted or unsubstituted C 5 -C 24 cycloalkyl, substituted or unsubstituted C 5 -C 24 cycloalkenyl, C(═O)R, OR, NRR′, C(═O) NRR′, OC(═O)R, CN, SR, S(═O) 2 R, S(═O) 2 OH and S(═O) 2 OM, wherein M is an alkali metal, or
R 7 and R 8 together with the carbon atoms to which they are bonded form an unsaturated or aromatic 5- to 20-membered carbocyclic ring that optionally contains 1, 2 or 3 heteroatom(s) selected from O, N or S as ring member(s);
Y is selected from the group consisting of hydrogen, halogen, O, —NR″, or S, wherein R″ is selected from the group consisting of hydrogen, substituted or unsubstituted, linear or branched C 1 -C 24 alkyl, substituted or unsubstituted, linear or branched C 2 -C 24 alkenyl, substituted or unsubstituted C 6 -C 24 aryl, substituted or unsubstituted C 7 -C 24 arylalkyl, substituted or unsubstituted C 5 -C 24 cycloalkyl and substituted or unsubstituted C 5 -C 24 cycloalkenyl; with the proviso that in case Y is hydrogen or halogen, then R 6 is not present; and
R and R′ are independently selected from the group consisting of hydrogen, substituted or unsubstituted, linear or branched C 1 -C 24 alkyl, substituted or unsubstituted, linear or branched C 2 -C 24 alkenyl, substituted or unsubstituted C 5 -C 24 cycloalkyl, substituted or unsubstituted C 5 -C 24 cycloalkenyl, substituted or unsubstituted C 6 -C 24 aryl and substituted or unsubstituted C 7 -C 24 arylalkyl;
comprising at least the steps of:
i) reacting at least one compound of formula (C)

wherein LG is halogen, O—S(═O) 2 CF 3 or O—S(═O) 2 CH 3 ;
with at least one compound of formula (B1)

wherein R 1 , R 2 , R 3 , R and R 5 are defined as above;
in the presence of at least one acid to obtain a compound of formula (D)

wherein Ar 1 and Ar 2 are defined as above;
ii) reacting the compound of formula (D) obtained according to step i) with at least one metal hydroxide to obtain a compound of formula (E)

wherein Ar 1 and Ar 2 are defined as above;
iii) reacting the compound of formula (E) obtained according to step ii) with at least one halogenating reagent to obtain a compound of formula (F)

wherein Ar 1 and Ar 2 are defined as above, and
W is selected from the group consisting of F, Cl, and Br; and
iv) reacting at least one compound of formula (F) obtained according to step iii) and at least one compound of formula (G),

wherein Y, Q, R 6 , R 7 , R 8 and R 9 are defined as above,
in the presence of an at least one acid to obtain a compound of formula (A).

2. The process according to claim 1 , comprising a step of:
v) reacting the product obtained according to step iv) with at least one alkyl halide or at least one acyl halide in presence of a base to obtain a compound of formula (A).

3. The process according to claim 1 , wherein in step (i) the at least one acid is selected from the group consisting of inorganic acids, Lewis acids, and organic acids.

4. The process according to claim 3 , wherein in step (i) the Lewis acids are selected from the group consisting of
AsX 3 , GaX 3 , BX 3 , BX 3 ·(C 2 H 5 ) 2 O, BX 3 ·S(CH 3 ) 2 , AlX 3 , (C 2 H 5 ) 2 AlX, SbX 3 , SbX 5 , SnX 2 , MgX 2 , MgX 2 ·O(C 2 H 5 ) 2 , ZnX 2 , BiX 3 , FeX 2 , TiX 2 , TiX 4 , NbX 5 , NiX 2 , CoX 2 , HgX 2 , PbX 2 , MnX 2 , CuX, CuX 2 whereby X in each case denotes F, Cl, Br, CF 3 —S(═O) 2 O, CH 3 —S(═O) 2 O, or I;
BH 3 , B(CH 3 ) 3 , GaH 3 , AlH 3 , Al(acetate)(OH) 2 , Al[OCH(CH 3 ) 2 ] 3 , Al(OCH 3 ) 3 , Al(OC 2 H 5 ) 3 , Al 2 O 3 , (CH 3 ) 3 Al, Ti[OCH (CH 3 ) 2 ] 3 Cl, Ti[OCH (CH 3 ) 2 ] 4 , methylaluminum di-(2,6-di-tert-butyl-4-methylphenoxide), methylaluminum di-(4-bromo-2,6-di-tert-butylphenoxide), LiClO 4 , Mg(acetate) 2 , Zn(acetate) 2 , Ni(acetate) 2 , Ni(NO 3 ) 2 , Co(acetate) 2 , Co(NO 3 ) 2 , Cu(acetate) 2 , Cu(NO 3 ) 2 , Li(acetate), Zr(acetylacetonate) 4 , Si(acetate) 4 , K(acetate), Na(acetate), Cs(acetate), Rb(acetate), Mn(acetate) 2 , Fe(acetate) 2 , Bi(acetate) 3 , Sb(acetate) 3 , Sr(acetate) 2 , Sn(acetate) 2 , Zr(acetate) 2 , Ba(acetate) 2 , Hg(acetate) 2 , Ag(acetate), Tl(acetate) 3 , Sc(trifluoromethanesulfonate) 3 , Ln(trifluoromethanesulfonate) 3 , Ni(trifluoromethanesulfonate) 2 , Ni(tosylate) 2 , Co(trifluoromethanesulfonate) 2 , Co(tosylate) 2 , Cu(tri-fluoromethanesulfonate) 2 and Cu(tosylate) 2 .

5. The process according to claim 4 , wherein in step (i) the at least one Lewis acid is selected from the group consisting of BX 3 , BX 3 ·(C 2 H 5 ) 2 O, BX 3 ·S (CH 3 ) 2 , AlX 3 , ZnX 2 , FeX 3 and TiX 4 , whereby X in each case denotes F, Cl, or Br.

6. The process according to claim 1 , wherein in step (i) the molar ratio of the at least one acid to the at least one compound of formula (C) is in the range of 1:10 to 10:1.

7. The process according to claim 1 , wherein in step (i) the molar ratio of the at least one compound of formula

Assignees

• Basf Se

Inventors

• Garg Rahul
• Patel Mushtaq
• Kolambkar Prachin
• Kadam Mileen
• Makade Deepak
• Bhatta Ramraj

Classifications

• C07D251/24 Primary

  to three ring carbon atoms · CPC title