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Triethylamine → Ethyl 3-methyl-4-oxobutanoate

HRID 638100
ノート
印刷プレビュー

反応式

HRID 638100 の反応式
[CH3:1][CH:2]([CH:9]=C)[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[O:11]=[O+][O-].C(N(CC)CC)C>C(Cl)Cl>[CH3:1][CH:2]([CH:9]=[O:11])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 24823OzoneHCID 12476290Ethyl 3-methylpent-4-enoate

生成物 1

HCID 13000833Ethyl 3-methyl-4-oxobutanoate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 53.18 g of 3A in 400 ml of dry methylene chloride was cooled to -78° C. Ozone was passed through the cold solution for 3.5 hours, air was passed through the solution for 10 minutes, then the solution was allowed to warm. At -50° C., 41.63 g of triethylamine was added drop-by-drop slowly. A strongly exothermic reaction occurred immediately, and the mixture was maintained at 5°-10° C. over the period of addition of the amine (30 minutes). The mixture then was stirred at room temperature for 2 hours, the solvents were evaporated under reduced pressure, and the residue was vacuum-chromatographed on silica gel, ether being used as eluent. The solution thus obtained was dried (MgSO4) and the solvent was evaporated to give ethyl 3-methyl-4-oxobutanoate (3B), as a slightly unstable pale yellow oil.

後処理

  1. temperatureto warm
  2. customA strongly exothermic reaction
  3. customthe solvents were evaporated under reduced pressure
  4. customthe residue was vacuum-chromatographed on silica gel, ether being
  5. customThe solution thus obtained
  6. dry with materialwas dried (MgSO4)
  7. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-5b6025f038014cd585f69244eedff1e4
出典データセット
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04560401

反応ノート

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