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Benzoyl chloride → HCID 21873086, 화합물

HRID 614861
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HRID 614861 반응식
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:10][C:11]([Cl:20])([Cl:19])[CH:12]([NH2:18])[NH:13][C:14](=[O:17])[CH2:15][Cl:16].C(N(CC)CC)C>CC(C)=O>[Cl:10][C:11]([Cl:19])([Cl:20])[CH:12]([NH:18][C:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[NH:13][C:14](=[O:17])[CH2:15][Cl:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7412Benzoyl chlorideHCID 8471TriethylamineHCID 53803331HCID 53803331, 화합물

생성물 1

HCID 21873086HCID 21873086, 화합물

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

Benzoyl chloride (4.7g) in acetone (5ml) was added dropwise to a solution of 1,1,1-trichloro-2-amino-2-(chloroacetamido)ethane (8g) in acetone (50ml) containing triethylamine (3.4g). The temperature rose to 50°. The mixture was stirred for 2 hours. The salt was filtered off and the filtrate poured into water. The solid formed was collected, washed with water and dried (10g). Recrystallisation from nitromethane gave pure 1,1,1-trichloro-2-benzamido-2-(chloroacetamido)ethane (8.7g. m.p. 211°-213°).

후처리

  1. customrose to 50°
  2. filtrationThe salt was filtered off
  3. additionthe filtrate poured into water
  4. customThe solid formed
  5. customwas collected
  6. washwashed with water
  7. dry with materialdried (10g)
  8. customRecrystallisation from nitromethane

출처 및 근거

ORD 기록
ord-823455765c3649189f32ac5781a7902e
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04146646

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