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

Methanol → Carbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl ester

HRID 869243
Notes
Print preview

Reaction equation

HRID 869243 reaction equation
[CH3:1][C:2]1([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.CO.C([O-])=O.[NH4+:22]>[Pd].O>[NH2:22][CH:5]1[CH2:6][CH2:7][C:2]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:1])[CH2:3][CH2:4]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 887MethanolHCID 2723923Ammonium formateHCID 21882608tert-butyl N-(1-methyl-4-oxocyclohexyl)carbamate

Product 1

HCID 20754832Carbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl esterYield 92.8%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalyst
HCID 962
Water
Solvent

Procedure

To a mixture of tert-butyl (1-methyl-4-oxocyclohexyl)carbamate (4.00 g) and methanol (50 mL), ammonium formate (10.2 g) and water (5 mL) were added and stirred for 1 hour until they were completely dissolved. Then, 10% palladium on carbon (2.0 g) was added and stirred at room temperature for 65 hours. After insoluble materials were separated by filtration through celite, the solvent was distilled off, and chloroform was added to the resulting residue, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off to give tert-butyl (4-amino-1-methylcyclohexyl)carbamate (3.73 g) as a colorless syrup.

Workup

  1. additionwere added
  2. dissolutionwere completely dissolved
  3. stirringstirred at room temperature for 65 hours
  4. customAfter insoluble materials were separated by filtration through celite
  5. distillationthe solvent was distilled off
  6. additionchloroform was added to the resulting residue
  7. dry with materialby drying over anhydrous magnesium sulfate
  8. distillationThe solvent was distilled off

Sources & evidence

ORD record
ord-2cbd4b36e7ae45179ab9477a99b5524e
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08969336B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes