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Bromine → 5-(2-Bromoacetyl)-1,3-phenylene diacetate

HRID 1699541
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인쇄 미리보기

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HRID 1699541 반응식
[C:1]([O:4][C:5]1[CH:6]=[C:7]([C:15](=[O:17])[CH3:16])[CH:8]=[C:9]([O:11][C:12](=[O:14])[CH3:13])[CH:10]=1)(=[O:3])[CH3:2].[Br:18]Br>C(=S)=S>[C:12]([O:11][C:9]1[CH:8]=[C:7]([C:15](=[O:17])[CH2:16][Br:18])[CH:6]=[C:5]([O:4][C:1](=[O:3])[CH3:2])[CH:10]=1)(=[O:14])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 6880155-Acetyl-1,3-phenylene diacetate

생성물 1

HCID 187073195-(2-Bromoacetyl)-1,3-phenylene diacetate

시약·촉매·용매 1

HCID 6348Carbon Disulfide용매2회

반응 조건

온도
50 °C

실험 절차

4 g of 3′,5′-diacetyloxyacetophenone was suspended in 75 ml of carbon disulfide. Thereto was dropwise added a solution of 0.90 ml of bromine dissolved in 25 ml of carbon disulfide, at room temperature in about 1 hour. The system was heated to about 50° C. ocassionally in the course of dropwise addition and, each time when a reaction started, the system was returned to room temperature and stirred. After the completion of the dropwise addition, stirring was conducted at room temperature for 1 hour. After the completion of the reaction, the solvent was removed by distillation to obtain 5.53 g of 3′,5′-diacetyloxy-2-bromoacetophenone as brown crystals.

후처리

  1. customwas returned to room temperature
  2. additionAfter the completion of the dropwise addition
  3. stirringstirring
  4. customAfter the completion of the reaction
  5. customthe solvent was removed by distillation

출처 및 근거

ORD 기록
ord-682ce54f10da4eb9b5b55e2fbdafe877
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE037556E1

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