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-Butanol → 2-Hydroxydecyl-butyl ether

HRID 267606
ノート
印刷プレビュー

反応式

HRID 267606 の反応式
[Na].[CH2:2]([OH:6])[CH2:3][CH2:4][CH3:5].[O:7]1[CH:9]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH2:8]1>>[OH:7][CH:9]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH2:8][O:6][CH2:2][CH2:3][CH2:4][CH3:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 2631-ButanolHCID 169931,2-EpoxydecaneHCID 5360545Sodium2 回

生成物 1

HCID 104664152-Hydroxydecyl-butyl ether収率 87%

反応条件

温度
100 °C

実験手順

0.46 gm (0.02 gm-atom) of sodium were added to 185 gm (2.5 mols) of n-butanol. After dissolution of the sodium, the temperature was raised to 100°C, and an amount of 78.2 gm (0.5 mol) of 1,2-epoxy decane was added in drops within 30 minutes while stirring. The reaction mixture was maintained at 100°C for 4 hours. Then the excess alcohol was distilled, and by subsequent vacuum distillation at 100° to 120°C and 0.06 Torr . the 2-hydroxy-decyl-n-butyl ether was separated from the higher boiling by-product. In this manner the intermediate product 2-hydroxydecyl-n-butyl ether (refractive index nD20 = 1.4392) was obtained in a yield of 87%.

後処理

  1. temperatureThe reaction mixture was maintained at 100°C for 4 hours
  2. distillationThen the excess alcohol was distilled
  3. distillationby subsequent vacuum distillation at 100° to 120°C
  4. customthe 2-hydroxy-decyl-n-butyl ether was separated from the higher boiling by-product

出典と根拠

ORDレコード
ord-69818f78eb614490b23a55445d05aee6
出典データセット
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03943178

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート