HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Chloroacetyl chloride → (S)-2-Chloro-N-(2,3-dihydroxypropyl)acetamide

HRID 556872
Notes
Print preview

Reaction equation

HRID 556872 reaction equation
C(N(CC)CC)C.[NH2:8][CH2:9][C@H:10]([OH:13])[CH2:11][OH:12].[Cl:14][CH2:15][C:16](Cl)=[O:17]>CC#N.CO>[Cl:14][CH2:15][C:16]([NH:8][CH2:9][C@H:10]([OH:13])[CH2:11][OH:12])=[O:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6577Chloroacetyl chlorideHCID 8471TriethylamineHCID 4409023-Amino-1,2-propanediol, (S)-

Product 1

HCID 11378718(S)-2-Chloro-N-(2,3-dihydroxypropyl)acetamideYield 90%

Reagents, catalysts & solvents 1

HCID 21959252Acetonitrile methanolSolvent

Procedure

Triethylamine (4.0 ml, 28.9 mmol) was added to a solution of (S)-3-amino-1,2-propanediol (2.2 g, 24.1 mmol) in a mixture of CH3CN/MeOH (80 mL/13 mL) at −10° C. under nitrogen. Chloroacetyl chloride (2.1 mL, 26.5 mmol) was then added dropwise at −10° C. over 30 min. The reaction mixture was allowed to reach room temperature and stirred for 16 h. The mixture was concentrated under vacuum and purified by flash column chromatography on silica gel, eluting with methanol/ethyl acetate (8/92), to give the title compound as a white solid (3.63 g, 90%).

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customto reach room temperature
  2. concentrationThe mixture was concentrated under vacuum
  3. custompurified by flash column chromatography on silica gel
  4. washeluting with methanol/ethyl acetate (8/92)

Sources & evidence

ORD record
ord-bdcb195f63e64282909f4dfe884f2e9e
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08058045B2

Reaction notes

Loading…