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

Hydrogen Bromide → 14-Bromo-1-tetradecanol

HRID 1367773
ノート
印刷プレビュー

反応式

HRID 1367773 の反応式
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][OH:15].[BrH:17]>C1CCCCC1>[Br:17][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][OH:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 260Hydrogen BromideHCID 882611,14-Tetradecanediol

生成物 1

HCID 275718214-Bromo-1-tetradecanol収率 67%

試薬・触媒・溶媒 1

HCID 8078Cyclohexane溶媒

実験手順

1,14-Tetradecandiol (1.5 g) was dissolved in 16.5 ml of cyclohexane, and 57% aqueous hydrobromic acid solution (16.5 ml) was added to this solution. The reaction mixture was refluxed for six hours while stirring. After the reaction, the mixture was extracted three times with diethyl ether. The organic layer was neutralized with saturated sodium hydrogen carbonate solution, washed with saline solution, dried over magnesium sulfate, and filtered, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel flash chromatography (hexane:ethyl acetate=7:3) gave 14-bromotetradecan-1-ol as white crystals at a 67% yield.

後処理

  1. temperatureThe reaction mixture was refluxed for six hours
  2. customAfter the reaction
  3. extractionthe mixture was extracted three times with diethyl ether
  4. washwashed with saline solution
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. distillationthe solvent was distilled off under reduced pressure
  8. customPurification of the residue by silica gel flash chromatography (hexane:ethyl acetate=7:3)

出典と根拠

ORDレコード
ord-4077f7eb98eb4a8f980d641aa157079d
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07893304B2

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