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Hydrochloric Acid → 3-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid

HRID 1367474
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반응식

HRID 1367474 반응식
C[O:2][C:3]([CH:5]1[CH2:9][CH2:8][CH:7]([S:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[Cl:19])(=[O:12])=[O:11])[CH2:6]1)=[O:4].[Li+].[OH-].Cl>CO>[Cl:19][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[S:10]([CH:7]1[CH2:8][CH2:9][CH:5]([C:3]([OH:4])=[O:2])[CH2:6]1)(=[O:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 669185503-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid methyl ester

생성물 1

HCID 669186983-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 3-(2-chloro-benzenesulfonyl)-cyclopentanecarboxylic acid methyl ester (0.25 g, 1.0 eq) in methanol (8.0 mL) was treated with 1N LiOH (1.6 mL, 2.0 eq). The mixture was stirred at RT for 3 h and then acidified to pH 4 with HCl 1N. The methanol was evaporated and the residue extracted with ethyl acetate. The organic phase was dried over sodium sulfate and evaporated. The title compound was obtained as a colorless oil (0.25 g, 100%) and was used crude. MS (ESI): m/z=287.3 [M−H]−.

후처리

  1. customThe methanol was evaporated
  2. extractionthe residue extracted with ethyl acetate
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customevaporated

출처 및 근거

ORD 기록
ord-0566d617b2754440a6374232642a4f02
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07893099B2

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