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3-Chloroaniline → HCID 54693832, 화합물

HRID 2292002
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HRID 2292002 반응식
[OH:1][C:2]1[C:3]2[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:4]=2[S:5][C:6]=1[C:7]([O:9]C)=O.[Cl:16][C:17]1[CH:18]=[C:19]([CH:21]=[CH:22][CH:23]=1)[NH2:20]>CCOCC>[OH:1][C:2]1[C:3]2[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:4]=2[S:5][C:6]=1[C:7]([NH:20][C:19]1[CH:21]=[CH:22][CH:23]=[C:17]([Cl:16])[CH:18]=1)=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 79323-ChloroanilineHCID 54693830Benzo[b]thiophene-2-carboxylic acid, 5-chloro-3-hydroxy-, methyl ester

생성물 1

HCID 54693832HCID 54693832, 화합물수율 56.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
170 °C

실험 절차

A mixture of methyl 3-hydroxy-5-chlorobenzo[b]thiophene-2-carboxylate (1.21 g; 0.005M) and 3-chloroaniline (1.28 g; 0.010M) is heated under a nitrogen atmosphere at 170° C. for 90 minutes. The reaction mixture was cooled to room temperature, taken up in 10 ml of ether, collected the solid, washed with 10 ml of ether, air dried, and recrystallized from ethyl acetate to give 0.95 g (56% yield) of the title compound as a light grey solid, m.p. 233°-235° C. (dec).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customcollected the solid
  3. washwashed with 10 ml of ether, air
  4. customdried
  5. customrecrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-b41c64df5a5e415e8d837b155dc8cf6d
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04800211

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