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Sodium Carbonate → 5-Amino-5-methylheptan-3-one

HRID 839995
ノート
印刷プレビュー

反応式

HRID 839995 の反応式
C(C1(C)N=[C:7]([CH2:9][CH3:10])[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4]1)C.C(=O)([O-])[O-:16].[Na+].[Na+]>Cl>[NH2:4][C:5]([CH3:11])([CH2:12][CH3:13])[CH2:6][C:7](=[O:16])[CH2:9][CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10340Sodium CarbonateHCID 205278902,4,6-Triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine

生成物 1

HCID 213304575-Amino-5-methylheptan-3-one

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

196.3 g of 2,4,6-triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine were added dropwise to 300 ml of concentrated hydrochloric acid at 30° - 40° C, with stirring. When the addition was complete, the mixture was stirred for a further 4 - 5 hours and then neutralized with sodium carbonate and extracted with benzene. The resulting benzene solution was washed with, in turn, a 5% aqueous solution of sodium carbonate and water, and was then dried over potassium carbonate. After removal of benzene, the residue was distilled under reduced pressure, giving 72.4 g of 5-amino-5-methyl-3-heptanone (bp 46° - 48° C/2.5 mmHg).

後処理

  1. additionWhen the addition
  2. stirringthe mixture was stirred for a further 4 - 5 hours
  3. extractionextracted with benzene
  4. washThe resulting benzene solution was washed with, in turn
  5. dry with materiala 5% aqueous solution of sodium carbonate and water, and was then dried over potassium carbonate
  6. customAfter removal of benzene
  7. distillationthe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-26d4840fd9a34dd684296857809976ea
出典データセット
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04097587

反応ノート

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