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Sodium Hydroxide → 5-Ethyl-2-(2-nitroanilino)thiophene-3-carboxylic acid

HRID 427034
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인쇄 미리보기

반응식

HRID 427034 반응식
[CH2:1]([C:3]1[S:7][C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N+:15]([O-:17])=[O:16])=[C:5]([C:18]([O:20]CC)=[O:19])[CH:4]=1)[CH3:2].[OH-].[Na+]>C(O)C.O>[CH2:1]([C:3]1[S:7][C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N+:15]([O-:17])=[O:16])=[C:5]([C:18]([OH:20])=[O:19])[CH:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 12442327Ethyl 5-ethyl-2-(2-nitroanilino)-thiophene-3-carboxylate

생성물 1

HCID 124389605-Ethyl-2-(2-nitroanilino)thiophene-3-carboxylic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

Ethyl 5-ethyl-2-(2-nitroanilino)-thiophene-3-carboxylate (6.0 g) dissolved in ethanol (100 ml) and water (50 ml) and heated to 60° C. with stirring. Sodium hydroxide (5 N, 50 ml) was then added and the temperature maintained for 16 hours. The reaction mixture was cooled and diluted with water (500 ml), and solid title product filtered off, m.p. 189°-191° C. (EtOAc).

후처리

  1. temperaturethe temperature maintained for 16 hours
  2. temperatureThe reaction mixture was cooled

출처 및 근거

ORD 기록
ord-af7f29731a024c599811bbb25d66b2d2
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04172831

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