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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070958Generated: November 3, 2026

Methyl iodide → Benzyl 3-bromo-5-cyanophenyl(methyl)carbamate

https://huagongshe.com/reaction/2070958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantbenzyl N-(3-bromo-5-cyanophenyl)carbamateHCID 68671401—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 3-bromo-5-cyanophenyl(methyl)carbamateHCID 6867110624.2%

Reaction Steps

To a stirring solution of 773 mg (2.33 mmol) of benzyl 3-bromo-5-cyanophenylcarbamate in 10 mL of THF at 0° C. was added 231 mg of NaH (60% dispersion in mineral oil). After 1 h, 300 μL (4.82 mmol) of methyl iodide was added, the ice bath was removed, and the red mixture was stirred at r.t. with the light off. After 17 h, saturated NH4Cl, H2O, and EtOAc were added and the layers separated. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (5% EtOAc/hexanes) provided 195 mg of benzyl 3-bromo-5-cyanophenyl(methyl)carbamate in 24% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-abc508fc16a946feba9062cd6f7f8b72
Source noteuspto-grants-2012_10