反応式
[CH:1]1([C:11](OC)=[O:12])[CH2:6][CH2:5][CH:4]([C:7](OC)=[O:8])[CH2:3][CH2:2]1.[H][H]>[Cr].[Cu]>[CH:1]1([CH2:11][OH:12])[CH2:6][CH2:5][CH:4]([CH2:7][OH:8])[CH2:3][CH2:2]1参加物
反応条件
- 温度
- 260 °C
実験手順
250 Parts of dimethyl 1,4-cyclohexanedicarboxylate and 25 parts of a copper-chromium catalyst were placed in an autoclave having a volume of 2 liters, and the mixture was stirred at 260° C. and reduced with hydrogen under a hydrogen pressure of 15 MPa. Then, the catalyst was removed by filtration, methanol formed as a side product was removed from an obtained filtrate by concentration, and the remaining filtrate was distilled under reduced pressure (160-175° C./1.33-2.00×103 Pa), to give 1,4-cyclohexanedimethanol (to be sometimes referred to as “CHDM” hereinafter). This product was subjected to 1H-NMR (JNM-AL400 supplied by JEOL) to show an isomer structure ratio of 71% of a trans-isomeric compound and 29% of a cis-isomeric compound (CHDM1).
後処理
- customThen, the catalyst was removed by filtration, methanol
- customformed as a side product
- customwas removed from an obtained filtrate by concentration
- distillationthe remaining filtrate was distilled under reduced pressure (160-175° C./1.33-2.00×103 Pa)
出典と根拠
- ORDレコード
- ord-12d2fe2ea7e247f4a62de3335e4f6962
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06780965B2
関連ノート
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