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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718688Generated: October 29, 2026

Methyl iodide → Methyl 2-(4-bromophenyl)-2-methylpropanoate

https://huagongshe.com/reaction/718688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantMethyl 2-(4-bromophenyl)propanoateHCID 11032083—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-bromophenyl)-2-methylpropanoateHCID 3651431—

Reaction Steps

To a stirred solution of compound 68b (5 g, 0.02 mol) in THF (100 mL) was added a 1 M THF solution of NaHMDS (22.6 mL, 22.6 mmol) at 0° C. under a nitrogen atmosphere. The resulting solution was allowed to warm to room temperature and stirred for 1 h. The reaction mixture was then cooled to 0° C. and iodomethane (3.19 g, 22.5 mmol) was added dropwise. The ice-water bath was removed and stirring was continued for an additional hour at room temperature. The reaction mixture was then treated with water (50 mL) and extracted with EtOAc (3×100 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to afford compound 68c as brown oil. Mass Spectrum (GCMS, ESI pos.): Calcd. for C11H13BrO2: 256.0 (M). found: 256.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-a12629057336446c8ce8053f9053c7c4
Source noteuspto-grants-2015_11