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Sodium Hydroxide → 4-((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)benzoic acid

HRID 747773
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인쇄 미리보기

반응식

HRID 747773 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:25]=[CH:24][C:18]([C:19]([O:21]CC)=[O:20])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>C(O)C>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:16]=[CH:17][C:18]([C:19]([OH:21])=[O:20])=[CH:24][CH:25]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 11783050tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate

생성물 1

HCID 27946494-((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)benzoic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

847 mg (2.43 mmol) of ethyl 4-(1-t-butoxycarbonyl-4-piperidyloxy)benzoate was dissolved in 50 ml of ethanol, and 5 ml of 1 N sodium hydroxide was added thereto, and they were stirred for 3 days. The reaction solution was concentrated and treated in an ordinary manner with ethyl acetate as the extractant to obtain the title compound.

후처리

  1. concentrationThe reaction solution was concentrated
  2. additiontreated in an ordinary manner with ethyl acetate as the extractant

출처 및 근거

ORD 기록
ord-c8232475ad78417ba480eb76be01816d
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396844B1

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