Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515488Generated: October 29, 2026

Triethylamine → HCID 66718654, compound

https://huagongshe.com/reaction/515488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloropropionyl chlorideHCID 111019—
Reactant3-{[(4-Methoxyphenyl)methyl]amino}propan-1-olHCID 5100981—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 66718654HCID 6671865478.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(4-methoxy-benzylamino)-propan-1-ol (2.00 g, 10.2 mmol) in dichloromethane (30 ml) was added triethylamine (1.09 g, 10.8 mmol) and 2-chloropropionyl chloride (1.37 g, 10.8 mmol) at 0° C. The mixture was stirred at 0° C. for one hour and partitioned between 0.5N hydrochloric acid and dichloromethane. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved into 2-propanol (50 ml) and potassium hydroxide (1.15 g, 20.5 mmol) was added at 0° C. The resulting mixture was stirred at 0° C. for 4 hours and partitioned between saturated ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluant: hexane/ethyl acetate=3/1) to afford 4-(4-methoxybenzyl)-2-methyl-[1,4]oxazepan-3-one as colorless oil (2.00 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108957B2
Source datasetuspto-grants-2015_08
ORD IDord-32035f3e702c4cb79fb967634ef75f59
Source noteuspto-grants-2015_08