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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
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Water → ST50668002

HRID 234495
ノート
印刷プレビュー

反応式

HRID 234495 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[CH2:10]([N:12]([CH2:16][CH3:17])[C:13](Cl)=[O:14])[CH3:11].O.CCOC(C)=O>N1C=CC=CC=1>[CH2:10]([N:12]([CH2:16][CH3:17])[C:13]([N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1)=[O:14])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6916Diethylcarbamoyl chlorideHCID 8857Ethyl AcetateHCID 10328Indoline

生成物 1

HCID 2987329ST50668002

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A solution of 6 g of indoline in 10 ml of pyridine is cooled to 0° C., 6.4 ml of diethylcarbamoyl chloride are added dropwise and the mixture is stirred for 18 hours at RT. Water is added to the reaction mixture, extraction is carried out with AcOEt, the organic phase is washed with water and with a 5% solution of potassium hydrogensulfate and dried over sodium sulfate and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using DCM as the eluent to give 8 g of the expected product, which is used as such.

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

後処理

  1. washthe organic phase is washed with water and with a 5% solution of potassium hydrogensulfate
  2. dry with materialdried over sodium sulfate
  3. customthe solvent is evaporated off under vacuum
  4. customThe residue is chromatographed on silica

出典と根拠

ORDレコード
ord-aa3c81db24384ac5970958029fc02e5c
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05594023

反応ノート

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