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Acetyl chloride → N-(2,4,5-Trichlorophenyl)acetamide

HRID 1577620
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HRID 1577620 반응식
[C:1](Cl)(=[O:3])[CH3:2].[Cl:5][C:6]1[CH:12]=[C:11]([Cl:13])[C:10]([Cl:14])=[CH:9][C:7]=1[NH2:8]>ClCCl>[CH3:2][C:1]([NH:8][C:7]1[C:6]([Cl:5])=[CH:12][C:11]([Cl:13])=[C:10]([Cl:14])[CH:9]=1)=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 124872,4,5-Trichloroaniline

생성물 1

HCID 90217N-(2,4,5-Trichlorophenyl)acetamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
50 °C

실험 절차

Acetyl chloride (2.13 mls; 0.03 mole) is added dropwise to a suspension of 2,4,5-trichloroaniline (4.91 g; 0.025 mole) and powdered 3A molecular sieves (7.4 g) in dichloromethane (25 mls), at room temperature, under a nitrogen atmosphere. When addition is completed, the mixture is heated to 50° C. for 1.5 hours and then cooled to room temperature. The 3A sieves are separated by filtration and washed with dichloromethane. All dichloromethane solutions are combined and evaporated to obtain 4.1 grams (69% of theoretical) of the solid product; m.p. 188°-190° C. after recrystallized from toluene.

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후처리

  1. customat room temperature
  2. additionWhen addition
  3. temperaturecooled to room temperature
  4. customThe 3A sieves are separated by filtration
  5. washwashed with dichloromethane
  6. customevaporated
  7. customto obtain 4.1 grams (69% of theoretical) of the solid product
  8. customm.p. 188°-190° C. after recrystallized from toluene

출처 및 근거

ORD 기록
ord-55fa5f57c1224c8aa63b76b6d398bdcc
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04288592

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