Triethylborane → Ethyl 6-(benzenesulphonylmethyl)-3-ethyl-2-methoxybenzoate
반응식
[CH2:1](C1C=C2C(COC2=O)=CC=1)[CH3:2].[C:13]1([S:19]([CH2:22][C:23]2[C:28]([C:29]([O:31][CH2:32][CH3:33])=[O:30])=[C:27]([O:34][CH3:35])[C:26](Br)=[CH:25][CH:24]=2)(=[O:21])=[O:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(B(CC)CC)C>>[C:13]1([S:19]([CH2:22][C:23]2[C:28]([C:29]([O:31][CH2:32][CH3:33])=[O:30])=[C:27]([O:34][CH3:35])[C:26]([CH2:1][CH3:2])=[CH:25][CH:24]=2)(=[O:21])=[O:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1참가 물질
4
실험 절차
Prepared by proceeding in a similar manner to Intermediate 18, starting from ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 61) and triethylborane.
후처리
- customPrepared
출처 및 근거
- ORD 기록
- ord-8ca5a2effad84c3381fa89dcf695823f
- 출처 데이터셋
- uspto-grants-2015_06
- 특허 번호
- US09067905B2
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