Docosanoic Acid → Behenyl behenate
Reaction equation
[C:1]([OH:24])(=[O:23])[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][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[CH2:25](O)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH3:46]>>[C:1]([O:24][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH3:25])(=[O:23])[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][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]Participants
3
Reactant 2
Product 1
Conditions
- Temperature
- 130 °C
Procedure
A four-necked rounded bottom flask equipped with a stirrer, a thermocouple, and a nitrogen inlet tube was charged with 1 mol of behenic acid per mol of behenyl alcohol, and the contents were heated to 130° C. for 3 hours in a nitrogen atmosphere to carry out an esterification reaction. A reaction product was purified with methyl ether to provide behenyl behenate. Here, the acid value was 0.1 mgKOH/g, and the hydroxyl value was 1.2 mgKOH/g
Workup
- customA four-necked rounded bottom flask equipped with a stirrer
- customan esterification reaction
- customA reaction product was purified with methyl ether
Sources & evidence
- ORD record
- ord-01f40b83c3e945a188fde6a54faa81a4
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921022B2
Reaction notes
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