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

Sodium Hydroxide → 3-(Pyrrolidine-1-carbonyl)thiomorpholine

HRID 326755
Notes
Print preview

Reaction equation

HRID 326755 reaction equation
[OH-].[Na+].Cl.[N:4]1([C:9]([CH:11]2[CH2:16][S:15][CH2:14][CH2:13][NH:12]2)=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5]1>C(Cl)Cl>[N:4]1([C:9]([CH:11]2[CH2:16][S:15][CH2:14][CH2:13][NH:12]2)=[O:10])[CH2:5][CH2:6][CH2:7][CH2:8]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 189150223-(Pyrrolidine-1-carbonyl)thiomorpholine monohydrochloride

Product 1

HCID 157301463-(Pyrrolidine-1-carbonyl)thiomorpholineYield 83.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A 1N aqueous sodium hydroxide solution (12.5 ml) was added to a mixture of 2.47 g of 3-(pyrrolidine-1-carbonyl)thiomorpholine monohydrochloride and 20 ml of methylene chloride. The organic layer was extracted and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to yield 1.75 g (83%) of 3-(pyrrolidine-1-carbonyl)thiomorpholine

Workup

  1. extractionThe organic layer was extracted
  2. dry with materialdried over anhydrous magnesium sulfate
  3. customThe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-c51eba5ded984a67bf21a23a08f822ac
Source dataset
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05270327

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes