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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323292Generated: October 25, 2026

Methyl phenylacetate → Methyl 3-cyano-2-phenylpropanoate

https://huagongshe.com/reaction/323292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl phenylacetateHCID 7559—
ReactantBromoacetonitrileHCID 11534—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-cyano-2-phenylpropanoateHCID 18464584—

Reaction Steps

Combine methyl phenylacetate (2.0 g, 13.32 mmol) and tetrahydrofuran (15 mL). Cool in a dry-ice/acetone bath. Add dropwise a solution of lithium diisopropylamide (6.66 mL, 2 M in THF, 13.32 mmol). After 1 hour, add α-bromoacetonitrile (1.6 g, 13.32 mmol). After 2 hours, warm the reaction mixture to ambient temperature and partition the reaction mixture between ethyl acetate and water. Separate the aqueous layer and extract three times with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and concentrate in vacuo to obtain a residue. Distill the residue bulb-to-bulb to give the title compound: bp; 150° C. at 0.5 mm Hg; Rf=0.72 (silica gel, 25% ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-94c4d080b6c14409865112be5c287e5b
Source noteuspto-grants-2001_04