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Water → 2-(4-Aminophenyl)-1lambda6,2-thiazolidine-1,1-dione

HRID 1268819
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인쇄 미리보기

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HRID 1268819 반응식
O.[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:15][CH2:14][CH2:13][S:12]2(=[O:17])=[O:16])=[CH:7][CH:6]=1)([O-])=O>O1CCCC1>[NH2:2][C:5]1[CH:6]=[CH:7][C:8]([N:11]2[CH2:15][CH2:14][CH2:13][S:12]2(=[O:17])=[O:16])=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 184468302-(4-Nitrophenyl)isothiazolidine 1,1-dioxide

생성물 1

HCID 118166852-(4-Aminophenyl)-1lambda6,2-thiazolidine-1,1-dione

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

1.0 g of water-moist Raney nickel is added to a solution of 2.60 g (10.7 mmol) of 2-(4-nitrophenyl)isothiazolidine 1,1-dioxide in 50 ml of tetrahydrofuran, and the mixture is hydrogenated at room temperature. The catalyst is filtered off, and the filtrate is evaporated, giving 2-(4-aminophenyl)isothiazolidine 1,1-dioxide as a brownish solid; ESI 213.

후처리

  1. customis hydrogenated at room temperature
  2. filtrationThe catalyst is filtered off
  3. customthe filtrate is evaporated

출처 및 근거

ORD 기록
ord-e4925122c8a64a0c8f61071a7e8aed62
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07199133B2

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