Ethyl 7-chloro-2-oxoheptanoate → ethyl (E)-7-chloro-((S)-2,2-dimethylcyclopropanecarboxamido)-2-heptenoate

HRID 2222779노트

반응식

HRID 2222779 반응식
ClCCCCCC(=O)C(OCC)=O.CC1(C)C[C@@H]1C(N)=O.[Cl:22][CH2:23][CH2:24][CH2:25][CH2:26]/[CH:27]=[C:28](\[NH:34][C:35]([C@H:37]1[CH2:39][C:38]1([CH3:41])[CH3:40])=[O:36])/[C:29]([O:31][CH2:32][CH3:33])=[O:30]>>[Cl:22][CH2:23][CH2:24][CH2:25][CH2:26]/[CH:27]=[C:28](/[NH:34][C:35]([C@H:37]1[CH2:39][C:38]1([CH3:40])[CH3:41])=[O:36])\[C:29]([O:31][CH2:32][CH3:33])=[O:30]

참가 물질

4

실험 절차

As described in European Patent No. 48301, 250 g of ethyl 7-chloro-2-oxoheptanoate and 141 g of (S)-2,2-dimethyl cyclopropanecarboxamid were reacted and concentrated. In result, 372.4 g of ethyl (Z)-7-chloro-((S)-2,2-dimethylcyclopropanecarboxamido)-2-hepnoate (2) containing, by gas chromatography assay, 10.5% of ethyl (E)-7-chloro-((S)-2,2-dimethylcyclopropanecarboxamido)-2-heptenoate (3) was obtained.

후처리

  1. concentrationconcentrated
  2. customIn result

출처 및 근거

ORD 기록
ord-7893dcc369ee4b42a2f14bfca804083c
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07371897B1

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