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

Hydrochloric Acid → N,N-Dimethyl-N-((4-methyl-2-oxooxazolidin-4-yl)methyl)propan-1-aminium chloride

HRID 1023486
Notes
Print preview

Reaction equation

HRID 1023486 reaction equation
[CH3:1][N:2]([CH2:4][C:5]1([CH3:11])[CH2:9][O:8][C:7](=[O:10])[NH:6]1)[CH3:3].[CH2:12](I)[CH2:13][CH3:14].C(=O)([O-])[O-].[K+].[K+].[ClH:22]>CCO.O.[Ag-]=O>[Cl-:22].[CH3:1][N+:2]([CH3:3])([CH2:4][C:5]1([CH3:11])[CH2:9][O:8][C:7](=[O:10])[NH:6]1)[CH2:12][CH2:13][CH3:14]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 336431-IodopropaneHCID 593551734-((Dimethylamino)methyl)-4-methyloxazolidin-2-one

Product 1

HCID 68562483N,N-Dimethyl-N-((4-methyl-2-oxooxazolidin-4-yl)methyl)propan-1-aminium chloride

Reagents, catalysts & solvents 3

HCID 178418778
HCID 178418778, compound
Catalyst
HCID 702EthanolSolvent
HCID 962WaterSolvent

Conditions

Temperature
50 °C

Procedure

A solution of 4-((dimethylamino)methyl)-4-methyloxazolidin-2-one (1.03 g, 6.51 mmol) in EtOH (5 ml) was added propyl iodide (2.5 ml, 26 mmol) in a sealed tube was heated to 50° C. for 16 h, then 70° C. for 6 h, then cooled to RT. Potassium carbonate (300 mg, 2.1 mmol) was added, and the solution was heated to 70° C. for an additional 20 h, cooled to RT, and diluted with H2O (10 ml). Silver (I) oxide (850 mg, 3.67 mmol) was added, and stirred for 30 min, and then 6.0 M HCl (˜400 ul) added until the solution was pH 7. The suspension was filtered through Celite and evaporated. ESI/APCI expected for C10H21N2O2+: 201.16. Found: 201.

Workup

  1. temperaturecooled to RT
  2. temperaturethe solution was heated to 70° C. for an additional 20 h
  3. temperaturecooled to RT
  4. filtrationThe suspension was filtered through Celite
  5. customevaporated

Sources & evidence

ORD record
ord-2628598298b346cebf750e42d2afe0ea
Source dataset
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08722715B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes