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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propargyl bromide → 2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole

HRID 127508
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HRID 127508 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[S:10].C(=O)([O-])[O-].[K+].[K+].[CH2:17](Br)[C:18]#[CH:19]>CC(C)=O>[CH2:19]([S:10][C:2]1[NH:1][C:9]2[C:4]([CH:3]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:18]#[CH:17]
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참가 물질

5

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 30323102-Indolinethione

생성물 1

HCID 202847712-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole수율 98%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of the product (14.9 g) of the above (1) in acetone (250 ml) are added potassium carbonate (16.5 g) and propargyl bromide (14.3 g) successively and the mixture is stirred at room temperature for three hours. The precipitate is filtered off. The filtrate is condensed and extracted with ether after addition of water. The extract is washed with water, dried and evaporated to remove the solvent yielding an oily residue (23 g). The residue is chromatographed on a column of silica gel (100 g) and eluted with benzene-hexane. The eluate is condensed to give the tile compound as an oil (18.3 g). Yield: 98%

후처리

  1. filtrationThe precipitate is filtered off
  2. customcondensed
  3. extractionextracted with ether
  4. additionafter addition of water
  5. washThe extract is washed with water
  6. customdried
  7. customevaporated
  8. customto remove the solvent

출처 및 근거

ORD 기록
ord-6ef44c71cfa8464f8e6d519c2943171b
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04256640

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