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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → [(4-Trifluoromethyl-phenyl)-piperidin-4-yloxy]-acetic acid

HRID 511073
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인쇄 미리보기

반응식

HRID 511073 반응식
FC(F)(F)C(O)=O.C([O:12][C:13](=[O:32])[CH2:14][O:15][CH:16]1[CH2:21][CH2:20][N:19]([C:22]2[CH:27]=[CH:26][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:24][CH:23]=2)[CH2:18][CH2:17]1)(C)(C)C>ClCCl>[F:30][C:28]([F:29])([F:31])[C:25]1[CH:24]=[CH:23][C:22]([N:19]2[CH2:20][CH2:21][CH:16]([O:15][CH2:14][C:13]([OH:32])=[O:12])[CH2:17][CH2:18]2)=[CH:27][CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 58576326[1-(4-Trifluoromethyl-phenyl)-piperidin-4-yloxy]-acetic acid tert-butyl ester

생성물 1

HCID 58576204[(4-Trifluoromethyl-phenyl)-piperidin-4-yloxy]-acetic acid수율 100%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroacetic acid (2 mL) is added to a solution of [1-(4-trifluoromethyl-phenyl)-piperidin-4-yloxy]-acetic acid tert-butyl ester (769 mg; 2.14 mmol, prepared in accordance with Example 10) in dichloromethane (2 mL). The reaction mixture is stirred until complete conversion is observed, is then concentrated under reduced pressure and co-evaporated with toluene (10 mL) to yield the desired product (985 mg, 2.14 mmol).

후처리

  1. concentrationis then concentrated under reduced pressure and co-evaporated with toluene (10 mL)

출처 및 근거

ORD 기록
ord-e685df8617df4e7faf6eafdba7876f30
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096524B2

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