Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496631Generated: October 31, 2026

Benzyl Bromide → HCID 22321881, compound

https://huagongshe.com/reaction/496631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantMethyl 2-Bromo-4-nitrobenzoateHCID 15833211—
ReactantHCID 178528066HCID 178528066—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22321881HCID 22321881—

Reaction Steps

A solution of benzyl bromide (2.0 mL, 17.3 mmol) in THF (10 mL) was added dropwise at 0° C. to a stirred suspension of zinc dust (1.7 g, 26 mmol) in THF (10 mL) which had been activated according to the method described by Knochel (J.O.C. 53, 2392, 1988). The mixture was left to warm to ambient temperature and stir for 3 h. An aliquot (6.5 mmol) of the supernatent containing the benzyl zinc reagent was then added to a stirred solution of compound 27 (3.85 mmol) and Pd(dba)3 (0.0385 mmol) in THF (10 mL) at ambient temperature under argon. After 1 hr a second aliquot (6.5 mmol) of the benzyl zinc reagent was added. The resulting black reaction mixture was quenched with 2N HCl (250 mL) and extracted with Ethyl acetate (2×100 mL). The combined organics were washed with water (50 mL) and brine (50 mL), filtered through phase separating paper and evaporated to an orange gum. This was purified by chromatography on silica (Merck, 9385) eluting with 10% ethyl acetate/i-hexane to give methyl 2-benzyl-4-nitro-benzoic acid (compound 28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946468B1
Source datasetuspto-grants-2005_09
ORD IDord-2bb19d327dfe4fa6aa66ff12acbe89e9
Source noteuspto-grants-2005_09