Reaction equation
[CH:1](=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C=O.[CH2:12](NCCCC)CCC.C(O)(=O)CCCCCCCCC>>[CH2:12]=[C:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH:1]=[O:9]Participants
5
Conditions
- Temperature
- 95 °C
Procedure
A 2 L four-necked flask equipped with a stirrer, a thermometer and a reflux condenser was charged with 762 g (6.0 mol) of n-octanal, 520 g (6.4 mol) of a 37% by mass formaldehyde aqueous solution, 15 g (0.33 mol) of dibutyl amine and 10 g (0.06 mol) of decanoic acid, and the contents in the flask were stirred while heating at 95° C. After the elapse of 45 min, it was confirmed that no n-octanal was present in the raw mixture, and then the mixture was cooled and separated into two layers. The thus separated organic layer was subjected to distillation treatment, thereby obtaining 790 g (5.4 mol) of a-methylene octanal (purity as measured by gas chromatography: 95%) (yield based on theoretical amount: 90%).
Workup
- customA 2 L four-necked flask equipped with a stirrer
- customAfter the elapse of 45 min, it
- temperaturethe mixture was cooled
- customseparated into two layers
- distillationThe thus separated organic layer was subjected to distillation treatment
Sources & evidence
- ORD record
- ord-4587e73c346047e7ae98bdbb2f4f0c05
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07732644B2
Linked notes
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