Malonic Acid → 15-Methylhexadec-2-enoic acid
反応式
[CH3:1][CH:2]([CH3:16])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]C=O.[C:17](O)(=O)[CH2:18][C:19]([OH:21])=[O:20].N1C=CC=CC=1>>[CH3:1][CH:2]([CH3:16])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH:17]=[CH:18][C:19]([OH:21])=[O:20]参加物
4
実験手順
13-methyl-tetradecanaldehyde (56.5 g, 0.25 mole), malonic acid (26.5 g, 0.51 mole), and pyridine (30.8 ml, 0.374 mole) were added to a flask and refluxed with heating for 3 hours. After cooling down 30% sulfuic acid was added and the reaction mixture was stirred for 3 hours under ice bath and then extracted by diethyl ether. Diethyl ether was removed by evaporation and product was subject to vacuum fractional distillation and 170–172° C./1.0 mmHg fraction was collected as 15-methyl-2-hexadecenoic acid (50.9 g, yield rate 76%).
後処理
- temperaturerefluxed
- temperaturewith heating for 3 hours
- additionwas added
- extractionextracted by diethyl ether
- customDiethyl ether was removed by evaporation and product
- distillationwas subject to vacuum fractional distillation and 170–172° C./1.0 mmHg fraction
- customwas collected as 15-methyl-2-hexadecenoic acid (50.9 g, yield rate 76%)
出典と根拠
- ORDレコード
- ord-295a3875713942908477f0183817fe89
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07109364B2
反応ノート
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