Pentanal → Cyclopentanone, 2-(1-hydroxypentyl)-

HRID 1373490Notes

Reaction equation

[CH:1](=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[OH-].[K+].[C:9]1(=[O:14])[CH2:13][CH2:12][CH2:11][CH2:10]1>[OH-].[Na+].C(=C1CCCC1=O)CCCC.O>[OH:6][CH:1]([CH:10]1[CH2:11][CH2:12][CH2:13][C:9]1=[O:14])[CH2:2][CH2:3][CH2:4][CH3:5]

Participants

Conditions

Temperature: 15 °C

Procedure

Valeraldehyde having an acid value of 3.4 mg-KOH/g was used as the starting material. 719 g (8.55 mol) cyclopentanone, 325 g water and 2.8 g (0.034 mol) 48% NaOH were introduced into a 2-L four-necked flask, then the mixture was cooled to 15° C. under stirring, and 337 g (3.91 mol) valeraldehyde was added dropwise at the same temperature over 5 hours. Thereafter, the mixture was stirred at the same temperature for 3 hours. After the reaction was finished, the mixture was neutralized and analyzed in the same manner as in Example 1. The result indicated that the reaction mixture contained 562 g (3.30 mol) 2-(1-hydroxy-n-pentyl)cyclopentanone (yield 85.0%) and 9.5 g (0.063 mol) 2-pentylidene cyclopentanone.

Workup

stirringThereafter, the mixture was stirred at the same temperature for 3 hours

Sources & evidence

ORD record: ord-89652515fc9d4d4189a64be40abf68a5
Source dataset: uspto-grants-2007_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07161041B2

Reaction notes

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