Hydrochloric Acid → HCID 86749040、化合物

HRID 2210476ノート

反応式

HRID 2210476 の反応式
[OH:1][N:2]=[C:3]([CH2:18][CH:19]([CH3:21])[CH3:20])[C:4]([NH:6][CH:7]([C:13]([O:15]CC)=[O:14])[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:5].[OH-].[Na+].O.Cl>C(O)C>[CH2:11]([O:10][C:8](=[O:9])[CH:7]([NH:6][C:4](=[O:5])[C:3](=[N:2][OH:1])[CH2:18][CH:19]([CH3:20])[CH3:21])[C:13]([OH:15])=[O:14])[CH3:12]

参加物

6

反応物 4

HCID 313Hydrochloric Acid2 回HCID 962WaterHCID 14798Sodium HydroxideHCID 86747153HCID 86747153、化合物

生成物 1

HCID 86749040HCID 86749040、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

In to a solution of 29.19 g of diethyl N-(2-hydroxyimino-4-methylpentanoyl)aminomalonate in 200 ml of ethanol was added 2.8 g of sodium hydroxide and 200 ml of water, then the mixture was stirred at room temperature for 4 hours. The reaction mixture was neutralized with 10% hydrochloric acid, then concentrated. To the residue thus obtained was added 10% hydrochloric acid to make it acidified, then it was extracted with ethyl acetate, and the ethyl acetate layer was washed with water, an aqueous solution saturated with sodium chloride in this order, then dried with magnesium sulfate. The solvent was removed by distillation to obtain 23.0 of N-(2-hydroxyimino-4-methylpentanoyl)aminomalonic acid monoethyl ester.

後処理

  1. concentrationconcentrated
  2. customTo the residue thus obtained
  3. extractionit was extracted with ethyl acetate
  4. washthe ethyl acetate layer was washed with water
  5. dry with materialan aqueous solution saturated with sodium chloride in this order, then dried with magnesium sulfate
  6. customThe solvent was removed by distillation

出典と根拠

ORDレコード
ord-ef0d970507764459ad3add25e2ba9775
出典データセット
uspto-grants-1995_10
特許番号
US05459142

反応ノート

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