Dimethyl 1,4-cyclohexanedicarboxylate → 1,4-Cyclohexanedimethanol

HRID 1837203

反応式

HRID 1837203 の反応式
[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

4

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

  1. customThen, the catalyst was removed by filtration, methanol
  2. customformed as a side product
  3. customwas removed from an obtained filtrate by concentration
  4. 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

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