Chloride → Methyl 4-chloro-3-(chlorosulfonyl)benzoate
반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[S:11]([Cl:14])(=[O:13])=[O:12].[Cl-].[CH3:16]O>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:16])=[O:7])=[CH:4][C:3]=1[S:11]([Cl:14])(=[O:12])=[O:13]참가 물질
4
실험 절차
A round bottom flask was charged with 4-chloro-3-(chlorosulfonyl)benzoic acid (16.0 g, 63.24 mmol) and methanol (100 mL), and thinoyl chloride (9.3 mL, 126.5 mmol) was added slowly at 0° C. The reaction mixture was then heated to reflux for 1.5 hours. The volatiles were removed under reduced pressure, and the residue was diluted with water and extracted with EtOAc. The solvents were removed under reduced pressure to get the title compound as a solid.
후처리
- additionwas added slowly at 0° C
- temperatureThe reaction mixture was then heated
- temperatureto reflux for 1.5 hours
- customThe volatiles were removed under reduced pressure
- additionthe residue was diluted with water
- extractionextracted with EtOAc
- customThe solvents were removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-6f0667ae0f104694bb887cc47f59ed7c
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08946439B2
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