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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048853Generated: October 30, 2026

Benzylethanolamine → Ethyl (4-benzylmorpholin-2-yl)acetate

https://huagongshe.com/reaction/1048853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl (E)-4-bromobut-2-enoateHCID 5373944—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEthyl (4-benzylmorpholin-2-yl)acetateHCID 1258257137.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

2-(Benzylamino)ethanol (19.05 ml, 132 mmol) and triethylamine (18.44 ml, 132 mmol) was added to water (150 ml) and the resulting mixture was heated to reflux temperature. (E)-Ethyl 4-bromobut-2-enoate (18.24 ml, 132 mmol) was added dropwise for 10 min The resulting mixture was further maintained at reflux temperature for 5 h. The reaction mixture was cooled to 25° C. and added NaOH (5.29 g, 132 mmol) after that the solvent was removed by distillation under reduced pressure to give orange oil. Ethyl acetate (150 mL) was added and the resulting solution was washed with water (2×50 mL). Ethyl acetate was distilled off under reduced pressure to give crude compound (15 g). This crude compound was purified by flash chromatography (Biotage) using eluent 20% ethyl acetate in hexane to yield 13 g of pure title compound as colorless viscous oil. m/z 264.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382216B2
Source datasetuspto-grants-2016_07
ORD IDord-a78af227dd354035adb7a0f759ac4a99
Source noteuspto-grants-2016_07