Hydrochloric Acid → 3-[(Methoxycarbonyl)amino]butanoic acid

HRID 449438

反応式

HRID 449438 の反応式
Cl[C:2]([O:4][CH3:5])=[O:3].[NH2:6][CH:7]([CH3:14])[CH2:8][C:9]([O:11]CC)=[O:10].C(N(CC)CC)C.O.[OH-].[Li+].Cl>O1CCCC1.O>[CH3:5][O:4][C:2]([NH:6][CH:7]([CH3:14])[CH2:8][C:9]([OH:11])=[O:10])=[O:3]

参加物

8

実験手順

Methyl chloroformate (0.071 mL, 0.91 mmol) was added to a solution of ethyl 3-aminobutanoate (0.10 g, 0.76 mmol) (Aldrich, Cat. #E10556) and triethylamine (0.16 mL, 1.1 mmol) in tetrahydrofuran (2.0 mL) at r.t. After stirring at r.t. for 30 min, the mixture was diluted with water, and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was dissolved in methanol (3.0 mL) and water (1.0 mL). To the solution was added lithium hydroxide monohydrate (0.049 g, 1.2 mmol). The reaction mixture was stirred at r.t. overnight. The mixture was adjusted to pH=2 with aqueous HCl, and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over MgSO4, filtered and concentrated to afford the desired product.

後処理

  1. extractionextracted with ethyl acetate (3×10 mL)
  2. dry with materialThe combined organic layers were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. dissolutionThe residue was dissolved in methanol (3.0 mL)
  6. stirringThe reaction mixture was stirred at r.t. overnight
  7. extractionextracted with ethyl acetate (3×10 mL)
  8. dry with materialThe combined organic layers were dried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-ddff6cff70424a10861e859c93330974
出典データセット
uspto-grants-2013_07
特許番号
US08481732B2

関連ノート

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