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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromine → 5-Bromo-2,3-dihydro-1-benzothiophene

HRID 576364
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반응식

HRID 576364 반응식
[S:1]1[CH2:5][CH2:4][C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]1=2.[Br:10]Br.C(=O)([O-])O.[Na+]>ClCCl.[Fe]>[Br:10][C:7]1[CH:8]=[CH:9][C:2]2[S:1][CH2:5][CH2:4][C:3]=2[CH:6]=1
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참가 물질

6

반응물 3

HCID 24408BromineHCID 783192,3-Dihydrobenzo(b)thiopheneHCID 516892Sodium Bicarbonate

생성물 1

HCID 123415135-Bromo-2,3-dihydro-1-benzothiophene수율 63%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 6344Dichloromethane용매

실험 절차

Iron powder (10.4 mg, 1.47 mmol) was added to a solution of 2,3-dihydrobenzo[b]thiophene 112 (400 mg, 2.94 mmol) in dichloromethane (5.9 mL). Bromine (0.15 mL, 2.94 mmol) was added dropwise to the mixture with stirring under ice-cooling. This mixture was stirred at the same temperature for 30 minutes. Saturated aqueous sodium hydrogen carbonate solution was added to the mixture and this was extracted with dichloromethane. The organic layer was washed with water, dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to provide the desired product 113 (396 mg, 63%).

후처리

  1. temperaturecooling
  2. stirringThis mixture was stirred at the same temperature for 30 minutes
  3. extractionthis was extracted with dichloromethane
  4. washThe organic layer was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-de53561b2d9d4ec9b30364aa21aeac86
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09034921B2

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