Glycine → N-Chloroacetylglycine

HRID 569839

反応式

HRID 569839 の反応式
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].[OH-].[Na+].[Cl:8][CH2:9][C:10](Cl)=[O:11]>CCOCC>[Cl:8][CH2:9][C:10]([NH:1][CH2:2][C:3]([OH:5])=[O:4])=[O:11]

参加物

5

実験手順

Glycine (1.5 g, 20 mmol) was dissolved in 2N NaOH (25 ml, 50 mmol) and ether (20 ml) was added. Chloroacetyl chloride (2.26 g) dissolved in Et2O (20 ml) was added dropwise at 0° C. The mixture was stirred at 0° for 30 minutes and at room temperature 1 hour. The layers were separated and the water layer was washed with Et2O (2×20 ml). The water layer was then acidified to pH 2 with concentrated HCl and the product was extracted into EtOAc (3×50 ml). The combined EtOAc extracts were washed with brine, dried (MgSO4), and freed of solvent in vacuo to give title acid compound as a solid (2.56 g, 84%) which was used without further purification.

後処理

  1. additionwas added dropwise at 0° C
  2. customThe layers were separated
  3. washthe water layer was washed with Et2O (2×20 ml)
  4. extractionthe product was extracted into EtOAc (3×50 ml)
  5. washThe combined EtOAc extracts were washed with brine
  6. dry with materialdried (MgSO4)

出典と根拠

ORDレコード
ord-23aff94fff4f4992854c02a5465c4fe5
出典データセット
uspto-grants-1988_03
特許番号
US04734425

関連ノート

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