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Trifluoroacetic acid → HCID 86692505, 화합물

HRID 1748558
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반응식

HRID 1748558 반응식
[CH2:1]([O:3][C:4]([C:6]1([C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][N:17]=2)[CH2:15][CH2:14][C:9]2(OCC[O:10]2)[CH2:8][CH2:7]1)=[O:5])[CH3:2].FC(F)(F)C(O)=O>>[CH2:1]([O:3][C:4]([C:6]1([C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][N:17]=2)[CH2:15][CH2:14][C:9](=[O:10])[CH2:8][CH2:7]1)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 86692455HCID 86692455, 화합물

생성물 1

HCID 86692505HCID 86692505, 화합물수율 91.1%

실험 절차

To 8-(5-bromopyridin-2-yl)-1,4-dioxaspiro[4.5]decane-8-carboxylic acid ethyl ester (1.0 g) described in Reference Example 81 (2) was added trifluoroacetic acid (1.1 ml) at room temperature, and stirred at the same temperature for 2 hours. After completion of the reaction, the solvent and trifluoroacetic acid were evaporated. The obtained residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 1-(5-bromopyridin-2-yl)-4-oxocyclohexanecarboxylic acid ethyl ester (803 mg) as a colorless oil.

후처리

  1. customAfter completion of the reaction
  2. customthe solvent and trifluoroacetic acid were evaporated
  3. customThe obtained residue was purified with silica gel column chromatography (n-hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-e9be3f13b15146cb882ede3e77da3cf4
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150555B2

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