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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464021Generated: October 29, 2026

p-Bromochlorobenzene → HCID 14249972, compound

https://huagongshe.com/reaction/464021

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Buten-1-olHCID 69389—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 14249972HCID 1424997252%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of triphenyl phosphine (2.1 g, 8.0 mmole) in 300 ml of triethylamine and 30 ml of acetonitrile under nitrogen is added successively palladium (II) acetate (0.45 g, 2.0 mmole), 1-bromo-4-chlorobenzene (19.1 g, 110 mmole) and 3-buten-1-ol (7.21 g, 100 mmole) in a pressure tube. The tube is sealed and heated in an oil bath to 100° C. for 24 hr. The tube is opened under nitrogen, charged with additional palladium (II) acetate, resealed and heated 20 hr longer at 100°-120° C. The mixture is cooled, vented to nitrogen and partitioned between 300 ml of 2N hydrochloric acid and ether. The layers are separated and the aqueous layer is extracted with two additional volumes of ether. The combined ether extracts are washed with 2×100 ml portions of 2N hydrochloric acid and then dried over sodium sulfate. The filtered ether extract is concentrated under vacuum to give 12.7 g of crude product which is purified by chromatography on silica gel using toluene eluent. There is obtained 9.5 g of the title compound. Rf =0.77 (silica gel, toluene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04545995
Source datasetuspto-grants-1985_10
ORD IDord-77d486a5858d426ea1b7199dae512c12
Source noteuspto-grants-1985_10