Triethylamine → N-methyloxan-4-amine hydrochloride

HRID 506975Notes

Reaction equation

HRID 506975 reaction equation
[ClH:1].CN.[O:4]1[CH2:9][CH2:8][C:7](=O)[CH2:6][CH2:5]1.[CH2:11]([N:13](CC)CC)C>[Pd].CO>[ClH:1].[CH3:11][NH:13][CH:7]1[CH2:8][CH2:9][O:4][CH2:5][CH2:6]1

Participants

6

Conditions

Temperature
60 °C

Procedure

A mixture of methylamine hydrochloride (5.4 g), terahydro-4H-pyran-4-one (8 g), triethylamine (2.4 g), 5% palladium on carbon (400 mg) and methanol (56 ml) were stirred at 60° C. for 3 hours under a hydrogen atmosphere. The palladium on carbon was removed by filtration through diatomaceous earth (Celite®) and the resultant filtrate evaporated in vacuo to a cream solid. To this solid were added propan-2-ol (39 ml), methanol (10 ml) and diethyl ether (20 ml), the resultant suspension then allowed to stir at room temperature for 1 hour, the solid was collected by filtration, washed with diethyl ether (10 ml) and dried in vacuo at room temperature to give N-methyl-N-(tetrahydropyran-4-yl)amine hydrochloride (9.83 g) as a white solid; NMR Spectrum: (DMSOd6) 1.62 (m, 2H); 1.94 (m, 2H); 2.53 (m, 3H); 3.14 (m, 1H); 3.3 (m, 2H); 3.91 (m, 2H); 9.24 (s, 2H).

Workup

  1. customThe palladium on carbon was removed by filtration through diatomaceous earth (Celite®)
  2. customthe resultant filtrate evaporated in vacuo to a cream solid
  3. additionTo this solid were added propan-2-ol (39 ml), methanol (10 ml) and diethyl ether (20 ml)
  4. stirringto stir at room temperature for 1 hour
  5. filtrationthe solid was collected by filtration
  6. washwashed with diethyl ether (10 ml)
  7. customdried in vacuo at room temperature

Sources & evidence

ORD record
ord-7e6ebd379fb54724ae9c2ad946e800c4
Source dataset
uspto-grants-2010_08
Patent number
US07786115B2

Reaction notes

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