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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975284Generated: November 1, 2026

Benzene → 3-(3-Bromopropyl)benzonitrile

https://huagongshe.com/reaction/1975284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBromide ionHCID 259—
ReactantTriphenylphosphineHCID 11776—
Reactant3-(3-Hydroxypropyl)benzonitrileHCID 13854262—
SolventAcetonitrileHCID 6342—
Product3-(3-Bromopropyl)benzonitrileHCID 19377230101.1%

Reaction Steps

To a mixture of 21.8 g (0.083 moles) of triphenyl phosphine stirred in 30 ml acetonitrile, 13.2 g (4.26 ml) bromide in 75 ml acetonitrile was added dropwise with stirring in an ice bath. After the addition was complete, the ice bath was removed and the mixture warmed to room temperature. Then a mixture of 12.1 g (0.075 mole) of 3-(3-cyanophenyl)-1-propanol (the product of step (b)) in 30 ml acetonitrile was added dropwise. The resulting mixture was allowed to warm to about 45°-50° C., was stirred overnight and then stripped. Benzene (50 ml) was added to the residue; the mixture was evaporated. Then, additional benzene (50 ml) was added. The mixture was stirred, and then filtered to remove the triphenyl phosphine. The filtrate was stripped to give an oil. The oil was chromatographed using a column containing 3.5 inches of 200 mesh silica gel (Merck) eluting with benzene, until TLC showed that no further product was eluted from the column. The eluates were pooled and stripped to give 17 g of an oil. The oil was distilled in a Kugelrohr apparatus, the fraction bpt. 102°-103° C. was collected to give 15.7 g of the above-identified product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286252
Source datasetuspto-grants-1994_02
ORD IDord-e2162ae5132b45bea7d8d2c17f54713f
Source noteuspto-grants-1994_02