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Bromine → HCID 23343672, 화합물

HRID 27175
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HRID 27175 반응식
[C:1]1(=[O:21])[N:5]([CH2:6][C:7]2[S:8][C:9]([C:12](=[O:15])[CH2:13][CH3:14])=[CH:10][CH:11]=2)[C:4](=[O:16])[C:3]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:2]12.[Br:22]Br>C(Cl)Cl>[Br:22][CH:13]([CH3:14])[C:12]([C:9]1[S:8][C:7]([CH2:6][N:5]2[C:4](=[O:16])[C:3]3=[CH:17][CH:18]=[CH:19][CH:20]=[C:2]3[C:1]2=[O:21])=[CH:11][CH:10]=1)=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 233436752-Phthalimidomethyl-5-propionylthiophene

생성물 1

HCID 23343672HCID 23343672, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2-Phthalimidomethyl-5-propionylthiophene (39.3 g., 0.13 mole) is dissolved in methylene chloride 300 ml.) and bromine (20.8 g., 0.13 mole) is added dropwise with stirring over 3/4 hours at room temperature. The solution is partially evaporated in vacuo to remove the hydrogen bromide. Then it is washed with saturated sodium carbonate solution and with water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. This affords 5-(2-bromopropionyl)-2-(phthalimidomethyl) thiophene as a pale beige solid (46.7 g.), m.p. 127°-130° C.

후처리

  1. customThe solution is partially evaporated in vacuo
  2. customto remove the hydrogen bromide
  3. washThen it is washed with saturated sodium carbonate solution and with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9a555335c3d247efa8cafe6e3ea787c1
출처 데이터셋
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04220654

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