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

Sodium Hydroxide → 1-(3-Amino-4',6'-dichlorophenyl)-pyrrolidin-2-one

HRID 848036
Notes
Print preview

Reaction equation

HRID 848036 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([NH:10][C:11](=[O:16])[CH2:12][CH2:13][CH2:14]Cl)[C:5]([Cl:9])=[CH:6][C:7]=1[Cl:8].[OH-].[Na+]>O1CCCC1>[NH2:1][C:2]1[CH:3]=[C:4]([N:10]2[CH2:14][CH2:13][CH2:12][C:11]2=[O:16])[C:5]([Cl:9])=[CH:6][C:7]=1[Cl:8]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 13062307N-(3-Amino-4,6-dichlorophenyl)-gamma-chlorobutyramide

Product 1

HCID 130623081-(3-Amino-4',6'-dichlorophenyl)-pyrrolidin-2-one

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

13.5 g (0.05 mol) of N-(3-amino-4,6-dichlorophenyl)-γ-chlorobutyramide, 200 ml of tetrahydrofurane and 100 ml of 1 N NaOH solution are stirred for 5 hours at 50° C. After the mixture has been allowed to cool, it is extracted three times with 300 ml of ethyl acetate and the extracts are washed with water, dried with magnesium sulphate and concentrated. The resulting product is recrystallised from toluene/ethyl acetate. Yield: 8.5 g; melting point 168°-170° C.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureto cool
  2. extractionit is extracted three times with 300 ml of ethyl acetate
  3. washthe extracts are washed with water
  4. dry with materialdried with magnesium sulphate
  5. concentrationconcentrated
  6. customThe resulting product is recrystallised from toluene/ethyl acetate

Sources & evidence

ORD record
ord-2c2b21ecf2b848f9bd3c00a20922cf99
Source dataset
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04294606

Reaction notes

Loading…