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

HRID 1421946
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인쇄 미리보기

반응식

HRID 1421946 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. occasionally 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-55f32c5ca21a442db67e5bf31cd2baa4
출처 데이터셋
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06080764

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