Furfural → Benzofuran

HRID 1643531ノート

反応式

HRID 1643531 の反応式
COC(/C=C/[C:7]1[CH:12]=[C:11](O)[C:10]2[O:14][CH:15](C3C=CC(O)=C(O)C=3)[CH:16](C(OC)=O)[C:9]=2[CH:8]=1)=O.O1C=CC=C1C=O.C(OCC)(=O)CCC(OCC)=O.CC(C)([O-])C.[K+].C([O-])(=O)C.[Na+].C(OC(=O)C)(=O)C.C([O-])([O-])=O.[K+].[K+]>CCO.C(O)(C)(C)C>[O:14]1[C:10]2[CH:11]=[CH:12][CH:7]=[CH:8][C:9]=2[CH:16]=[CH:15]1

参加物

10

反応物 7

HCID 7362Furfural2 回HCID 7918Acetic AnhydrideHCID 11430Potassium CarbonateHCID 31249Diethyl Succinate2 回HCID 517045Sodium AcetateHCID 5857314DihydrobezofuranHCID 23665647Potassium tert-butoxide

生成物 1

HCID 9223Benzofuran

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 6386tert-Butanol溶媒

実験手順

As depicted in Scheme F, dihydrobenzofuran intermediate F-3 could be prepared starting from commercially available 2-furaldehyde and diethyl succinate. Treatment of 2-furaldehyde and diethyl succinate with potassium t-butoxide in refluxing t-butanol gives intermediate F-1. Treatment of F-1 with sodium acetate in refluxing acetic anhydride, followed by aqueous work-up and subsequently refluxing the residue in EtOH in the presence of K2CO3, gives benzofuran F-2. F-2 could be subjected to hydrogenation conditions to provide dihydrobenzofuran F-3.

後処理

  1. customcould be prepared
  2. customgives intermediate F-1

出典と根拠

ORDレコード
ord-85cdb687fa3d4a11a8a9f11dec122a49
出典データセット
uspto-grants-2012_02
特許番号
US08119624B2

反応ノート

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