Glycine → N-Chloroacetylglycine

HRID 648625

Reaction equation

HRID 648625 reaction equation
[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]

Participants

5

Procedure

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.

Workup

  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)

Sources & evidence

ORD record
ord-2a23c6a9d1f04aa4888a978df0b8c03d
Source dataset
uspto-grants-1988_04
Patent number
US04735962

Linked notes

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