Hydrochloric Acid → N-Acetyl-S-methyl-L-cysteine

HRID 325330

反応式

HRID 325330 の反応式
[CH3:1][S:2][CH2:3][C@@H:4]([C:6]([OH:8])=[O:7])[NH2:5].[OH-].[Na+].[C:11](OC(=O)C)(=[O:13])[CH3:12].Cl>>[CH3:1][S:2][CH2:3][C@@H:4]([C:6]([OH:8])=[O:7])[NH:5][C:11](=[O:13])[CH3:12]

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 7918Acetic AnhydrideHCID 14798Sodium HydroxideHCID 24417(-)-S-Methyl-L-cysteine

生成物 1

HCID 13893975N-Acetyl-S-methyl-L-cysteine収率 80.6%

実験手順

S-Methyl-L-cysteine (119.6 g, 0.89 mole) was dissolved in 1.87 l (1.87 mole) of 1 N sodium hydroxide solution and then ice-cooled. Thereafter, 92.6 ml (0.98 mole) of acetic anhydride was added dropwise and the mixture was stirred for 2.0 hours at room temperature. The reaction mixture was acidified to pH 1.0 with 6 N hydrochloric acid and extracted with 1 liter of ethyl acetate five times. The extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo to give 126.4 g of S-methyl-N-acetyl-L-cysteine as an oil (80.6% yield). A second crop of 5.17 g (3.3%) was recovered by reextraction of the aqueous layer.

後処理

  1. temperatureice-cooled
  2. extractionextracted with 1 liter of ethyl acetate five times
  3. dry with materialThe extracts were dried over anhydrous magnesium sulfate
  4. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2aaa495b46bc4d9b8a75a64dde900409
出典データセット
uspto-grants-1984_04
特許番号
US04440788

関連ノート

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