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

HRID 45013

反応式

HRID 45013 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

7

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-9e846d06d04742b19e2be123854baf36
出典データセット
uspto-grants-2013_09
特許番号
US08541425B2

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