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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278860Generated: November 3, 2026

Water → 2-[3-(2-Morpholin-4-ylethoxy)phenyl]acetonitrile

https://huagongshe.com/reaction/1278860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantLithiumHCID 3028194—
ReactantMethyl 3-(2-morpholin-4-ylethoxy)benzoateHCID 7164628—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran heptane ethylbenzolHCID 22742125—
Product2-[3-(2-Morpholin-4-ylethoxy)phenyl]acetonitrileHCID 22262779—

Reaction Steps

Lithium diisopropylarmide (18.8 ml, 37 mmol, 2.0 M solution in heptane/tetrahydrofuran/ethylbenzene) was added dropwise to a solution of acetonitrile (1.58 g, 37 mmol) in dry tetrahydrofuran (50 ml) at −78° C. After stirring the reaction mixture for 30 min., a solution of methyl 3-(2-morpholin-4-ylethoxy)benzoate in dry tetrahydrofuran (50 ml) was added dropwise over 10 min. After 15 min., water was added and the reaction mixture was allowed to warm to room temperature. The aqueous layer was separated and acidified with dilute hydrochloric acid to pH 7. The product was extracted into ethyl acetate and washed with water and brine and dried over magnesium sulfate. The organics were removed in vacuo to give 2-[3-(2-morpholin-4-ylethoxy)phenyl]acetonitrile (5.0 g) as an oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444696B1
Source datasetuspto-grants-2002_09
ORD IDord-b5003a2ef39544948c8e990cb813884a
Source noteuspto-grants-2002_09