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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572563Generated: October 31, 2026

Methylamine → HCID 66652590, compound

https://huagongshe.com/reaction/572563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
Reactant4'-CyanoacetophenoneHCID 74044—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantSodium borohydrideHCID 4311764—
CatalystTitanium isopropoxideHCID 11026—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66652590HCID 66652590—

Reaction Steps

In THF (50 mL) was added 4-acetylbenzonitrile (5.0 g; 34 mmol), methylamine (21 mL; 2.00 M solution in THF; 42 mmol) and titanium isopropoxide (5.6 mL; 19 mmol). The mixture was stirred at RT overnight. Sodium borohydride (5.5 g; 145 mmol) was added and the reaction mixture was let stirred at RT for 2 h. Ammonium hydroxide solution 25% (100 mL) was added and the reaction mixture was stirred at RT for 1 h30. It was then filtered through a pad of celite, which was washed with EtOAc. The organic phase was washed with a saturated solution of NaHCO3, brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was then dissolved in CH3CN (41 mL). Potassium carbonate (10.3 g; 74 mmol) and tert-butyl bromoacetate (5.5 mL; 37 mmol) were added at RT and the reaction mixture was stirred at RT for 1 h30. EtOAc was added and the organic phase was washed with water and brine, dried over MgSO4, filtered and concentrated affording an oil which was purified by Flash Chromatography affording the title compound as a colorless oil. 1H NMR (DMSO-d6, 300 MHz) δ 7.79 (d, J=8.4 Hz, 2H), 7.54 (d, J=8.2 Hz, 2H), 3.89 (q, J=6.7 Hz, 1H), 3.27 (d, J=16.7 Hz, 1H), 3.07 (d, J=16.7 Hz, 1H), 2.21 (s, 3H), 1.41 (s, 9H), 1.26 (d, J=6.8 Hz, 3H). LC/MS (Method B): 275.1 (M+H)+. HPLC (Method A) Rt 2.83 min (Purity: 96.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029405B2
Source datasetuspto-grants-2015_05
ORD IDord-7b76564528234c189936bed23ca9714b
Source noteuspto-grants-2015_05