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Chloroacetonitrile → HCID 18924851, 화합물

HRID 1288818
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HRID 1288818 반응식
[NH2:1][C:2]1[S:3][C:4]([CH3:20])=[C:5]([CH3:19])[C:6]=1[C:7](=O)[C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([O:16][CH3:17])[CH:9]=1.[Cl:21][CH2:22][C:23]#[N:24].[Cl-].[Al+3].[Cl-].[Cl-]>>[Cl:21][CH2:22][C:23]1[N:24]=[C:7]([C:8]2[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([O:16][CH3:17])[CH:9]=2)[C:6]2[C:5]([CH3:19])=[C:4]([CH3:20])[S:3][C:2]=2[N:1]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7856ChloroacetonitrileHCID 858786HCID 858786, 화합물HCID 6451240Aluminum(III) Chloride

생성물 1

HCID 18924851HCID 18924851, 화합물수율 44%

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온도
100 °C

실험 절차

To a mixture of 2-amino-3-(3,4-dimethoxybenzoyl)-4,5-dimethylthiophene (3.0 g) and chloroacetonitrile (11 g) was added, in limited amounts, powdered aluminum chloride (2.75 g). The mixture was stirred for 2.5 hours at 100° C. The reaction mixture was poured into ice-water, which was subjected to extraction with chloroform. The chloroform layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, which was dried (MgSO4). Chloroform was distilled off, and the residue was subjected to column chromatography on silica gel. From the fraction eluted with dichloromethane, 2-chloromethyl-4-(3,4-dimethoxyphenyl)-5,6-dimethylthieno[2,3-d]pyrimidine (1.58 g, 44%) was obtained. Recrystallization from ethyl acetate-hexane gave colorless prisms, m.p.117°-118° C.

후처리

  1. extractionwas subjected to extraction with chloroform
  2. washThe chloroform layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, which
  3. dry with materialwas dried (MgSO4)
  4. distillationChloroform was distilled off
  5. washFrom the fraction eluted with dichloromethane

출처 및 근거

ORD 기록
ord-f92f0e4344ae4a7da45f8915a22684c2
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05747486

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