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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406980Generated: October 29, 2026

Methyl iodide → Ethyl 2-(4-bromophenyl)propanoate

https://huagongshe.com/reaction/406980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 2-(4-bromophenyl)acetateHCID 7020609—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-bromophenyl)propanoateHCID 13840376—

Reaction Steps

2.0 M LDA in heptane/THF/ethylbenzene (6.0 mL, 12 mmol) was slowly added to a solution of ethyl (4-bromophenyl)acetate (2.43 g, 10.0 mmol) in THF (20 mL) at −78° C. and then the mixture was stirred for 30 min. Methyl iodide (0.93 mL, 15 mmol) was added at −78° C. and then the reaction was stirred for an additional 30 min. Saturated NH4Cl aq. was added to quench the reaction. The mixture was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexane (0-10%) to afford the desired product (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754114B2
Source datasetuspto-grants-2014_06
ORD IDord-ea33d576172040488a0aefe9e7e83041
Source noteuspto-grants-2014_06