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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430955Generated: November 2, 2026

4-Methyloxybenzyl chloride → HCID 86708669, compound

https://huagongshe.com/reaction/1430955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 86708665HCID 86708665—
SolventDimethylformamideHCID 6228—
ProductHCID 86708669HCID 8670866976.2%

Reaction Steps

A solution of tert-butyl (4-bromo-2-chloro-5-cyanophenyl)carbamate (1.0 g, 3.02 mmol) in DMF (10 mL) was cooled in an icebath and NaHMDS (1 M solution in THF, 4.52 ml, 4.52 mmol) was added. After 20 min, 4-methoxybenzyl chloride (0.616 ml, 4.52 mmol) was added and the reaction was removed from the bath and left stirring at RT overnight. The reaction was partitioned between EtOAc and sat. aq. NH4Cl solution. The aqueous phase was extracted with EtOAc and the combined organic extracts were washed with brine. After drying with sodium sulfate, the solvents were removed and silica gel chromatography with hexane containing 0 to 30% EtOAc afforded tert-butyl (4-bromo-2-chloro-5-cyanophenyl)(4-methoxybenzyl)carbamate (1.04 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940736B2
Source datasetuspto-grants-2015_01
ORD IDord-7bcb37ce2cb44358a20bbb619434fe57
Source noteuspto-grants-2015_01