反応式
[C:1]([OH:10])(=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:11](O)[CH2:12][OH:13]>>[C:1]([O:10][CH2:11][CH2:12][OH:13])(=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]参加物
3
実験手順
Anhydride of caprylic acid (0.477 mol; 129 g) was dropwise added into boiling dry ethylene glycol (3.16 mol; 196 g) and the mixture was refluxed for further 4 hours. The mixture was cooled, extracted twice with benzene (100+20 ml), benzene was evaporated in a rotation evaporator, and the residue was distilled. 2-Hydroxyethyl caprylate was obtained in the yield of 142.75 g (159% of theory), which is the evidence that almost 2/3 of caprylic acid formed was esterified with glycol under the experimental conditions. The raw fractions had purity 88.9 to 97.5% of 2-hydroxyethyl caprylate. Further procedure was carried out according to example 1.
後処理
- temperaturethe mixture was refluxed for further 4 hours
- temperatureThe mixture was cooled
- extractionextracted twice with benzene (100+20 ml), benzene
- customwas evaporated in a rotation evaporator
- distillationthe residue was distilled
出典と根拠
- ORDレコード
- ord-d704a49c1ae44f66bd6a9553e55e7bf7
- 出典データセット
- uspto-grants-1990_08
- 特許番号
- US04950733
関連ノート
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