Ethanol → Ethyl 3,3-dimethylpent-4-enoate

HRID 359170

反応式

HRID 359170 の反応式
C(OC(OCC)(O[CH2:7][CH:8]=[C:9]([CH3:11])[CH3:10])C)C.[C:15]1([OH:21])C=CC=C[CH:16]=1.[CH2:22]([OH:24])[CH3:23]>>[CH3:10][C:9]([CH3:11])([CH:8]=[CH2:7])[CH2:23][C:22]([O:21][CH2:15][CH3:16])=[O:24]

参加物

4

反応物 3

HCID 702EthanolHCID 996PhenolHCID 133214151-(1,1-Diethoxyethoxy)-3-methylbut-2-ene

生成物 1

HCID 82262Ethyl 3,3-dimethylpent-4-enoate収率 72%

実験手順

A mixture of 2.02 g of 1,1-diethoxy-1-(3-methyl-2-buten-1-yloxy)ethane and 20 mg of phenol was heated for 12 hours at 150°-160°, during which time ethanol was evolved. Distillation of the residue gave 1.12 g (72% yield) of ethyl 3,3-dimethyl-4-pentenoate, b.p. 80°-83°/57 mm.

後処理

  1. distillationDistillation of the residue

出典と根拠

ORDレコード
ord-6660faa2fb4841c8a261dc641d29db7d
出典データセット
uspto-grants-1991_03
特許番号
US04999451

関連ノート

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