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2,5-Furandicarboxylic acid → Tetrahydrofuran-2,5-dicarboxylic acid

HRID 1889211
ノート
印刷プレビュー

反応式

HRID 1889211 の反応式
[O:1]1[C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=[C:2]1[C:9]([OH:11])=[O:10]>C(O)(=O)C>[O:1]1[CH:5]([C:6]([OH:8])=[O:7])[CH2:4][CH2:3][CH:2]1[C:9]([OH:11])=[O:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 767202,5-Furandicarboxylic acid

生成物 1

HCID 237334Tetrahydrofuran-2,5-dicarboxylic acid収率 88%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
140 °C

実験手順

A 100 mL pressure vessel with a glass liner and an impeller was charged with 1.87 g of furan-2,5-dicarboxylic acid, 0.5 g of 4% Pd/Silica and 40 mL of acetic acid. The pressure vessel was purged 3 times with nitrogen, and 2 times with hydrogen. The vessel was then pressurized to 750 psig hydrogen and heated to 140° C. for 3 hours. After cooling the vessel was vented and the solids were separated by filtration. The acetic acid solution was evaporated under vacuum to provide 1.68 g (88% yield) of tetrahydrofuran-2,5-dicarboxylic acid.

後処理

  1. customThe pressure vessel was purged 3 times with nitrogen, and 2 times with hydrogen
  2. temperatureAfter cooling the vessel
  3. customthe solids were separated by filtration
  4. customThe acetic acid solution was evaporated under vacuum

出典と根拠

ORDレコード
ord-2ef3cade6abc469697a8e598d34d196e
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501989B2

反応ノート

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