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[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]#N)=[C:7]([Cl:13])[CH:6]=1.C(O)=[O:16]>>[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]=[O:16])=[C:7]([Cl:13])[CH:6]=1참가 물질
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- 온도
- 110 °C
실험 절차
A solution of (3-chloro-4-cyano-phenyl)acetic acid methyl ester 13 (7.4 g, 35.3 mmol) in 88% formic acid (100 mL) is combined with Raney-alloy (9.0 g) and heated to reflux for 10 hours at 110° C. After cooling to room temperature, the alloy is removed by filtration over Celite. The filtrate is concentrated to ˜10% of the original volume and diluted with EtOAc (250 mL) and washed three times with water (80 mL). The organic layer is dried (MgSO4), filtered and concentrated to afford crude product, which is purified by silica gel chromatography using an EtOAc/hexane gradient to give (3-Chloro-4-formyl-phenyl)-acetic acid methyl ester 14 as a wax-like solid. Another amount of product 14 is collected by reesterification of saponified byproduct (3-Chloro-4-formyl-phenyl)-acetic acid: 1H-NMR (400 MHz, CDCl3) δ=10.31 (s, 1H), 7.84 (d, J=8.0 Hz, 1H), 7.58 (s, 1H), 7.45 (d, J=8.0 Hz, 1H), 3.86 (s, 3H), 3.64 (s, 2H). MS calculated for C10H10ClO3 (M+H+) 213.0, found 213.3.
후처리
- temperatureheated
- temperatureAfter cooling to room temperature
- customthe alloy is removed by filtration over Celite
- concentrationThe filtrate is concentrated to ˜10% of the original volume
- additiondiluted with EtOAc (250 mL)
- washwashed three times with water (80 mL)
- dry with materialThe organic layer is dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto afford crude product, which
- customis purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-d2bbdbb85910429bbc057a4e7fb8425c
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07820705B2
연결된 노트
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