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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 → HCID 23366165、化合物

HRID 1080886
ノート
印刷プレビュー

反応式

HRID 1080886 の反応式
[Cl:1][C:2]1[C:11]([Cl:12])=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:13](Cl)=[O:14])[CH:8]=2)[N:3]=1.[BH4-].[Na+].O>O1CCOCC1>[Cl:1][C:2]1[C:11]([Cl:12])=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH2:13][OH:14])[CH:8]=2)[N:3]=1
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 962WaterHCID 747146-Quinoxalinecarbonyl chloride, 2,3-dichloro-HCID 4311764Sodium borohydride

生成物 1

HCID 23366165HCID 23366165、化合物

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

To a suspension of 25.3 g portion of 2,3-dichloroquinoxaline-6-carbonyl chloride synthesized in accordance with the procedure disclosed in JP-A 57-98274 in 400 ml of anhydrous 1,4-dioxane, was added 14.0 g of sodium borohydride, and the mixture was stirred at room temperature for 10 minutes in an atmosphere of nitrogen. With cooling on an ice bath, to this was added dropwise 100 ml of water. Thereafter, 1,4-dioxane was evaporated under a reduced pressure, and the resulting residue was purified by chromatography on a silica gel column (eluent, hexane/ethyl acetate) to obtain 8.75 g of 2,3-dichloro-6-hydroxymethylquinoxaline.

後処理

  1. customsynthesized in accordance with the procedure
  2. temperatureWith cooling on an ice bath
  3. customThereafter, 1,4-dioxane was evaporated under a reduced pressure
  4. customthe resulting residue was purified by chromatography on a silica gel column (eluent, hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-2d182e9289154a7cb188372a3fe947cd
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05583227

反応ノート

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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