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Water → 4-(2-Hydroxyethyl)cyclohexan-1-ol

HRID 40982
ノート
印刷プレビュー

反応式

HRID 40982 の反応式
[OH:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][C:7](=[O:10])[CH2:6][CH2:5]1.[AlH4-].[Li+].O.[OH-].[Na+]>CCOCC.C1COCC1>[OH:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][CH:7]([OH:10])[CH2:6][CH2:5]1
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

7

反応物 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 28112Lithium aluminum hydrideHCID 157003924-(2-Hydroxyethyl)cyclohexan-1-one

生成物 1

HCID 137511534-(2-Hydroxyethyl)cyclohexan-1-ol

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒3 回
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

4-(2-Hydroxyethyl)cyclohexanone (2.00 g, 0.0141 mol) was dissolved in ether (30.00 mL) and was cooled at 0° C. To the reaction was added 1.0 M lithium tetrahydroaluminate in ether (14.1 mL) and the resulting mixture was stirred at 0° C. for 2 hours and at 25° C. for 16 hours. To the reaction was added THF (20.00 mL) and this mixture was cooled at 0° C. and then water (0.40 mL, 0.022 mol) was added, followed by 1.00 M sodium hydroxide (0.40 mL). To the reaction was then added ether (100.00 mL) and the resulting mixture was stirred for 10 minutes, then was filtered and the filtrate was concentrated using a rotary evaporator to provide the crude product. The crude product was used in the next reaction without further purification.

後処理

  1. temperaturethis mixture was cooled at 0° C.
  2. filtrationwas filtered
  3. concentrationthe filtrate was concentrated
  4. customa rotary evaporator

出典と根拠

ORDレコード
ord-80fda129872c4577b0185fdb7b5229dc
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530485B2

反応ノート

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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