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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505381Generated: October 25, 2026

3-Bromo-4-(phenylmethoxy)-benzonitrile → HCID 56984010, compound

https://huagongshe.com/reaction/1505381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-(phenylmethoxy)-benzonitrileHCID 3960018—
ReactantHCID 178418443HCID 178418443—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56984010HCID 56984010—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 1M solution of ethyl magnesium bromide (2 mL, 1.5 equiv), THF (10 mL) was added and the reaction mixture was cooled down to 0° C. A solution of 0.5 M in THF of zinc dichloride (4 mL, 1.5 equiv) was added slowly and the reaction mixture was stirred for 30 min at the same temperature. Pd(tBu3P)2 (102 mg, 0.1 equiv) was added followed by the addition of a solution of 3-bromo-4-[(phenylmethyl)oxy]benzonitrile (Intermediate 110, 576 mg) in THF and the reaction was allowed to reach room temperature. After stirring 30 minutes, some additional Pd(tBu3P)2 was added (51 mg, 0.05 equiv), then 30 min stirring, then third addition of Pd(tBu3P)2 (51 mg, 0.05 equiv) and stirring 30 min. The reaction mixture was quenched with an aqueous saturated solution of NH4Cl (100 mL) and extracted 3 times with ethyl acetate (3×150 mL). The gathered organic phases were filtrated on celite, dried over sodium sulphate. The residue obtained was purified by chromatography on silica gel (Companion system, 40 g Si cartridge) using as eluent a gradient cyclohexane/ethyl acetate 100:0, then 100:0 to 90:10. Evaporation afforded the title compound (336 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216967B2
Source datasetuspto-grants-2015_12
ORD IDord-6f496eeca2a247c39f1cb1f5d49538cf
Source noteuspto-grants-2015_12