Furfuryl Alcohol → Furfuryl Alcohol

HRID 2168857ノート

反応式

HRID 2168857 の反応式
[C:1](=[O:4])([OH:3])[OH:2].[CH2:5]([OH:11])[CH2:6][CH2:7][CH:8]([OH:10])[CH3:9].[CH2:12]([OH:18])[C:13]1[O:17][CH:16]=[CH:15][CH:14]=1>>[C:1](=[O:3])([O:2][CH2:9][C:8]1[O:11][CH:5]=[CH:6][CH:7]=1)[O:4][CH2:12][C:13]1[O:17][CH:16]=[CH:15][CH:14]=1.[C:1](=[O:2])([OH:4])[OH:3].[CH2:5]([OH:11])[CH2:6][CH2:7][CH:8]([OH:10])[CH3:9].[CH2:12]([OH:18])[C:13]1[O:17][CH:16]=[CH:15][CH:14]=1

参加物

5

反応物 2

HCID 7361Furfuryl AlcoholHCID 867022981,4-Pentanediol carbonate

生成物 3

HCID 7361Furfuryl AlcoholHCID 86702297HCID 86702297、化合物HCID 867022981,4-Pentanediol carbonate

実験手順

Adding 1,4-pentanediol carbonate and furfuryl alcohol in a tubular ester exchange reactor; then adding the prepared metal-rare earth oxide composite catalyst, mixing uniformly and performing an ester exchange reaction, distilling the reaction product to obtain difurfuryl carbonate, wherein the mole ratio of 1,4-pentanediol carbonate to furfuryl alcohol is 1:6, and the weight ratio of the metal-rare earth oxide composite catalyst to the total weight of 1,4-pentanediol carbonate and furfuryl alcohol is 0.5:100; the ester exchange reaction is performed at a temperature of 160° C. and under an absolute pressure of 3 MPa for 20 minutes; in the ester exchange reaction, the conversion rate of 1,4-pentanediol carbonate is 100%, and yield of difurfuryl carbonate is 92%.

後処理

  1. additionmixing uniformly
  2. distillationdistilling the reaction product

出典と根拠

ORDレコード
ord-1647cb1a0f394c4199a99504f8dfb8d6
出典データセット
uspto-grants-2015_06
特許番号
US09045707B2

反応ノート

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