Chloroacetic Acid → 3,7-dimethyloct-6-en-1-yl chloroacetate
反応式
[Cl:1][CH2:2][C:3]([OH:5])=[O:4].[CH3:6][CH:7]([CH2:11][CH2:12][CH:13]=[C:14]([CH3:16])[CH3:15])[CH2:8][CH2:9]O>[OH-].[K+].O>[CH2:9]([O:4][C:3](=[O:5])[CH2:2][Cl:1])[CH2:8][CH:7]([CH2:11][CH2:12][CH:13]=[C:14]([CH3:16])[CH3:15])[CH3:6]参加物
5
実験手順
A mixture of 94.5 g (1.0 mol) of monochloroacetic acid and 203.2 g (1.4 mol) of 3,7-dimethyl-6-octen-1-ol (citronellol) was heated for 6 h at 50 mbar to 130° C., wherein the water formed by esterification was distilled off via a column. The reaction mixture obtained had an acid value of 5 mg KOH/g. Unreacted citronellol was then distilled off at 6 mbar and a bottoms temperature of up to 130° C. Distillation of the residue at 6 mbar yielded 198 g of chloroacetic acid citronellyl ester as a colourless liquid.
後処理
- customformed by esterification
- distillationwas distilled off via a column
- customThe reaction mixture obtained
- distillationwas then distilled off at 6 mbar
- customup to 130° C
- distillationDistillation of the residue at 6 mbar
出典と根拠
- ORDレコード
- ord-ffc27537c5f74f5487be0f16c623ed3b
- 出典データセット
- uspto-grants-2007_06
- 特許番号
- US07229958B2
反応ノート
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