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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333272Generated: October 30, 2026

Methylamine → HCID 53323814, compound

https://huagongshe.com/reaction/333272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58954812HCID 58954812—
CatalystTitanium cation (4+)HCID 114942—
ProductHCID 53323814HCID 533238144.4%

Reaction Steps

A mixture of 1-(1-(3,4-dichlorophenyl)cyclohexyl)ethanone (247 mg, 0.91 mmol) and methyl amine (455 μL, 2.0 M in THF, 0.91 mmol) was stirred at RT for 2 min. Titanium (IV) isoproxide (336 μL, 1.14 mmol) was then added. The viscous green/yellow solution was stirred at RT for 3 h. NaBH3CN solution (640 μL, 1.0 M in MeOH, 0.64 mmol) was added and the cloudy solution was stirred at RT for 16 h. The solution was quenched with saturated NaCl solution (3 mL), filtered, and washed with MeOH (50 mL). 6M HCl (20 mL) was added and the aqueous phase was washed with Et2O (2×20 mL). The pH of the aqueous phase was adjusted to pH=12 with 3M NaOH and washed with EtOAc (3×30 mL). The combined organic phases were dried (Na2SO4), filtered and concentrated. To a solution of the crude amine in Et2O (3 mL) was added HCl (3 mL, 2.0 M in Et2O). The crude HCl salt was recrystallized from CH3CN (6 mL) at 110° c to give 1-(1-(3,4-dichlorophenyl)cyclohexyl)-N-methylethanamine (8 mg) as white crystals. HPLC Rt=8.90 min; 1H NMR (400 mHz, CD3OD) 7.57-7.53 (m, 2H), 7.33-7.31 (m, 1H), 3.15-3.13 (m, 2H), 2.61 (s, 3H), 2.45 (broad d, J=11.73 Hz, 1H), 2.30 (broad d, J=12.46, 1H), 1.59-1.51 (m, 5H), 1.31-1.08 (m, 6H); LC-MS 7.87 min, (M+1) 286 @ 8.10 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877975B2
Source datasetuspto-grants-2014_11
ORD IDord-c408d96133f04a4eb88c9d623b8ebb3c
Source noteuspto-grants-2014_11