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

1,4-Butanediol → 4-(2-Fluoro-5-bromobenzyloxy)butanol

HRID 1066815
ノート
印刷プレビュー

反応式

HRID 1066815 の反応式
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[H-].[Na+].[F:9][C:10]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:11]=1[CH2:12]Br>CN(C)C=O>[F:9][C:10]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:11]=1[CH2:12][O:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6]
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 80641,4-ButanediolHCID 24758Sodium hydrideHCID 135532954-Bromo-2-(bromomethyl)-1-fluorobenzene

生成物 1

HCID 211961624-(2-Fluoro-5-bromobenzyloxy)butanol

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of 1,4-dihydroxybutane (4.0 ml, 45.13 mmol) in N,N-dimethylformamide (62 ml) was treated with sodium hydride (1.98 g of a 60% solution, 49.63 mmol), and stirred for about 50 minutes at ambient temperature. The resulting mixture was cooled to 0° C. and treated with 2-fluoro-5-bromobenzyl bromide (3.0 g, 11.28 mmol). The reaction mixture was then stirred for four hours at ambient temperature. The reaction was quenched with water. The aqueous fraction was extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The desired title intermediate was further purified by high performance liquid chromatography.

後処理

  1. temperatureThe resulting mixture was cooled to 0° C.
  2. stirringThe reaction mixture was then stirred for four hours at ambient temperature
  3. customThe reaction was quenched with water
  4. extractionThe aqueous fraction was extracted with methylene chloride
  5. dry with materialdried over sodium sulfate
  6. customThe solvents were removed in vacuo
  7. customThe desired title intermediate was further purified by high performance liquid chromatography

出典と根拠

ORDレコード
ord-96ffe5c3cac14f118bd24bd99d6196d6
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06245761B1

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