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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39200Generated: October 28, 2026

Methyl iodide → 1,3-Diethyl 2-(4-bromophenyl)-2-methylpropanedioate

https://huagongshe.com/reaction/39200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl 4-bromophenylmalonateHCID 10519382—
SolventTetrahydrofuranHCID 8028—
Product1,3-Diethyl 2-(4-bromophenyl)-2-methylpropanedioateHCID 1061630755%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diethyl 2-(4-bromophenyl)malonate (1.5 g, 4.8 mmol) in dry THF (5 mL) at 0° C. was added sodium hydride (380 mg, 9.5 mmol). After stirring for 30 minutes at 0° C., iodomethane (600 μL, 9.5 mmol) was added and the reaction was allowed to warm to room temperature. After stirring for 12 h at room temperature, the reaction was quenched with water (3 mL). The mixture was partitioned between 1 N HCl (10 mL) and dichloromethane (10 mL), and the organic layer was separated. The organic layer was washed with 1 N HCl (10 mL), dried over Na2SO4 and evaporated. The crude material was purified by silica gel chromatography, eluting with 0-20% ethyl acetate in hexanes, to give diethyl 2-(4-bromophenyl)-2-methylmalonate (850 mg, 55%) 1H NMR (400 MHz, DMSO-d6) δ 7.59-7.55 (m, 2H), 7.31-7.27 (m, 2H), 4.21-4.14 (m, 4H), 1.75 (s, 3H), 1.19-1.16 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524767B2
Source datasetuspto-grants-2013_09
ORD IDord-16879a0a0bc44b89958b8465a906fb28
Source noteuspto-grants-2013_09