ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Propargyl bromide → 2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole

HRID 127508
ノート
印刷プレビュー

反応式

HRID 127508 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 30323102-Indolinethione

生成物 1

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

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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%

後処理

  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

出典と根拠

ORDレコード
ord-6ef44c71cfa8464f8e6d519c2943171b
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04256640

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート