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Hydrochloric Acid → 4-Methylpentane-2,3-dione 2-oxime

HRID 1169821
ノート
印刷プレビュー

反応式

HRID 1169821 の反応式
[CH3:1][CH:2]([C:4](=[O:7])[CH2:5][CH3:6])[CH3:3].Cl.[N:9](OCCC(C)C)=[O:10]>COC(C)(C)C.COCCOC>[CH3:1][CH:2]([CH3:3])[C:4](=[O:7])[C:5](=[N:9][OH:10])[CH3:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 112652-Methyl-3-pentanone

生成物 1

HCID 573574754-Methylpentane-2,3-dione 2-oxime

試薬・触媒・溶媒 2

HCID 80711,2-Dimethoxyethane溶媒HCID 15413tert-Butyl methyl ether溶媒2 回

実験手順

100 g (948 mmol) of 2-methylpentan-3-one were dissolved in 400 ml of tert-butyl methyl ether. 50 g (274 mmol) of solution of hydrochloride in ethylene glycol dimethyl ether (20%) were added. Subsequently, a solution of 117 g (949 mmol) isoamyl nitrite in 150 ml of tert-butyl methyl ether was added dropwise within 60 minutes. The solvent was removed fully under reduced pressure. The residue was taken up in 300 ml of n-heptane and concentrated again under reduced pressure. After 200 ml of n-heptane had been added, extraction was effected with 522 ml of sodium hydroxide solution (2 molar). After phase separation, the aqueous phase was washed with n-heptane. The aqueous phase was acidified by adding conc. hydrochloric acid. The product was isolated by filtration with suction, washed with water and dried at elevated temperature under reduced pressure.

後処理

  1. customThe solvent was removed fully under reduced pressure
  2. concentrationconcentrated again under reduced pressure
  3. additionAfter 200 ml of n-heptane had been added
  4. extractionextraction
  5. customAfter phase separation
  6. washthe aqueous phase was washed with n-heptane
  7. additionby adding conc. hydrochloric acid
  8. customThe product was isolated by filtration with suction
  9. washwashed with water
  10. customdried at elevated temperature under reduced pressure

出典と根拠

ORDレコード
ord-296dd41297e44329bd762c1e557fa588
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07825144B2

反応ノート

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