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Ethyl chloroformate → HCID 13020003, 화합물

HRID 1277830
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HRID 1277830 반응식
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:4]=[C:5]([CH:14]=[CH:15][CH:16]=1)[O:6][C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][CH:8]=1.Cl[C:20]([O:22][CH2:23][CH3:24])=[O:21]>N1C=CC=CC=1>[F:1][C:2]([F:17])([F:18])[C:3]1[CH:4]=[C:5]([CH:14]=[CH:15][CH:16]=1)[O:6][C:7]1[CH:8]=[CH:9][C:10]([NH:13][C:20](=[O:21])[O:22][CH2:23][CH3:24])=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10928Ethyl chloroformateHCID 27607504-[3-(trifluoromethyl)phenoxy]aniline

생성물 1

HCID 13020003HCID 13020003, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

4-[3-(trifluoromethyl)phenoxy]benzenamine (6.0 grams; 0.21 mol) and pyridine (50 ml) were placed in a glass reaction vessel equipped with a mechanical stirrer and placed in an ice bath. Ethyl chloroformate (5 ml) was added dropwise to the reaction mixture with continuous stirring. Stirring was continued overnight and the mixture was then poured into ice water (500 ml). The precipitate was washed with water and dried. It was found to have a melting point of 74°-75.5° C. In fraud analysis confirmed the identity of the desired product.

후처리

  1. customequipped with a mechanical stirrer
  2. customplaced in an ice bath
  3. washThe precipitate was washed with water
  4. customdried

출처 및 근거

ORD 기록
ord-4dd1c15ce9b9459bbf8b89c9e685a1cf
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04279637

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