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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741002Generated: October 30, 2026

Allyl bromide → HCID 70185477, compound

https://huagongshe.com/reaction/1741002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantHCID 21834382HCID 21834382—
SolventAcetonitrileHCID 6342—
ProductHCID 70185477HCID 7018547788%

Reaction Steps

The ethyl 3-(4-carboethoxyphenyl)propanol (1.00 g, 4.80 mmol) was dissolved in 8 ml of dry acetonitrile under nitrogen and treated with carbonyl diimidazole (1.01 g, 6.24 mmol). After ten minutes, allyl bromide (1.66 ml, 19.2 mmol) was added and the reaction was refluxed for 5 hours. After cooling, the mixture was evaporated, slurried in water and extracted twice with 5:1 pentane/diethyl ether solution. The organic extracts were washed with water and then brine, dried over MgSO4 and concentrated to afford 1.15 g (88% yield) of the subtitle compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972972
Source datasetuspto-grants-1999_10
ORD IDord-0dbdf0453c4a4dce8b83e6a0243ad315
Source noteuspto-grants-1999_10