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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249049Generated: October 26, 2026

Water → N-(2-Benzoyloxyethyl)-N-ethylamine

https://huagongshe.com/reaction/249049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-(N-ethylanilino)ethanolHCID 62338—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-Benzoyloxyethyl)-N-ethylamineHCID 1976277296%

Reaction Steps

Benzoyl chloride (7.8 mL, 66 mmol) was added dropwise to a stirring solution of (N-ethyl-N-(2-hydroxyethyl)aniline (10 g, 60 mmol) in THF (200 ML) containing triethyl amine (9.2 g, 66 mmol) at room temperature. The mixture formed a thick precipitate which was stirred for 18 hours and then poured into water (400 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL). The combined organic extracts were washed successively with 1 molar hydrochloric acid (100 mL), saturated sodium bicarbonate (100 mL), water (100 mL), saturated sodium chloride (100 mL), dried over magnesium sulfate and the solvent was removed under reduced pressure to yield the product (16.4 g, 96% yield) as a dark green oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212269
Source datasetuspto-grants-1993_05
ORD IDord-43ea3992753e40759df9faf134894b0e
Source noteuspto-grants-1993_05