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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370671Generated: October 30, 2026

Hexane → HCID 178444304, compound

https://huagongshe.com/reaction/370671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178444335HCID 178444335—
SolventDichloromethaneHCID 6344—
ProductHCID 178444304HCID 17844430478%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 16.6 g of tetrabromomethane in 230 ml of methylene chloride was placed at 0° C. in a sulphonation flask under an argon atmosphere and treated portionwise within 10 minutes with 26.2 g of solid triphenylphosphine; there thereby resulted a clear, deep orange solution. After completion of the addition, the mixture was stirred at 0° C. for a further 5 minutes and then a solution of 6.46 g of p-(trans-4-pentylcyclohexyl)benzaldehyde in 20 ml of methylene chloride was added dropwise within 10 minutes. After stirring at 0° C. for a further 1 hour, the orange mixture was poured into 750 ml of hexane and the precipitate which thereby separated was filtered off (rinsing with hexane). The concentrated filtrate (20.4 g) was digested with 250 ml of warm hexane, filtered (rinsing with warm hexane) and the filtrate was concentrated. Low-pressure chromatography (0.5 bar) of the residual oil (9.70 g) on silica gel with 3% ethyl acetate/petroleum ether gave 8.08 g (78%) of β,β-dibromo-p-(trans-4-pentylcyclohexyl)styrene as colourless crystals (purity 97.5%); m.p. 48° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528114
Source datasetuspto-grants-1985_07
ORD IDord-6faf4dc176054d52a5a548cfed5877fa
Source noteuspto-grants-1985_07