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Pyridine → 2-chloro-N-[4-chloro-3-(trifluoromethyl)phenyl]acetamide

HRID 1453792
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HRID 1453792 반응식
[Cl:1][CH2:2][C:3](Cl)=[O:4].[Cl:6][C:7]1[CH:13]=[CH:12][C:10]([NH2:11])=[CH:9][C:8]=1[C:14]([F:17])([F:16])[F:15].N1C=CC=CC=1>ClCCl>[Cl:1][CH2:2][C:3]([NH:11][C:10]1[CH:12]=[CH:13][C:7]([Cl:6])=[C:8]([C:14]([F:17])([F:15])[F:16])[CH:9]=1)=[O:4]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 6577Chloroacetyl chlorideHCID 675744-Chloro-3-(trifluoromethyl)aniline

생성물 1

HCID 23077292-chloro-N-[4-chloro-3-(trifluoromethyl)phenyl]acetamide수율 98.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

Chloroacetic acid chloride (0.69 ml; 8.44 mmol) is dropped slowly into a stirred solution of 4-chloro-3-trifluoro methyl aniline (1.5 g; 7.67 mmol) in pyridine (0.81 ml; 9.97 mmol) and dichloromethane (15 ml), cooled to 0° C. Stirring is continued for 2 h at room temperature. The reaction mixture is diluted with dichloromethane, washed twice with 1N aqueous hydrochloric acid and with water. The reaction mixture is then dried over Na2SO4, filtered and evaporated to yield 2.05 g (98%) brownish solid of 9.

후처리

  1. washwashed twice with 1N aqueous hydrochloric acid and with water
  2. dry with materialThe reaction mixture is then dried over Na2SO4
  3. filtrationfiltered
  4. customevaporated

출처 및 근거

ORD 기록
ord-30d3de86a9bc433d926c7be42cf49a6c
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07476683B2

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