Ethanol → Ethyl 3-oxohexanoate

HRID 2090588ノート

反応式

HRID 2090588 の反応式
[CH2:1]([CH:5]1C(=O)O[C:8](C)([CH3:12])[O:7][C:6]1=[O:14])[CH2:2][CH2:3][CH3:4].C([OH:17])C>>[O:17]=[C:1]([CH2:2][CH2:3][CH3:4])[CH2:5][C:6]([O:7][CH2:8][CH3:12])=[O:14]

参加物

3

反応物 2

HCID 702EthanolHCID 110634455-butyl-2,2-dimethyl-1,3-dioxane-4,6-dione

生成物 1

HCID 238498Ethyl 3-oxohexanoate収率 72%

実験手順

The 5-butyl-2,2-dimethyl-1,3-dioxane-4,6-dione thus obtained was allowed to reflux in ethanol for 2 hours, and then concentrated under reduced pressure. The resulting residue was purified using silica gel chromatography (developing solvent: n-hexane/ethyl acetate=8/2) to obtain the ethyl 3-oxohexanoate shown by the formula below.

後処理

  1. concentrationconcentrated under reduced pressure
  2. customThe resulting residue was purified

出典と根拠

ORDレコード
ord-126cd627a5554cf8ad46da2674d9cdd7
出典データセット
uspto-grants-2013_05
特許番号
US08436210B2

反応ノート

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