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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370679Generated: October 29, 2026

Hexane → HCID 178445832, compound

https://huagongshe.com/reaction/370679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178445835HCID 178445835—
SolventDichloromethaneHCID 6344—
ProductHCID 178445832HCID 17844583239.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 13.6 g of tetrabromomethane in 150 ml of methylene chloride was placed at 0° C. in a sulphonation flask under argon gasification and treated within 10 minutes with a solution of 21.51 g of triphenylphosphine in 40 ml of methylene chloride. After completion of the addition, the clear orange solution was stirred at 0° C. for a further 5 minutes and then a solution of 5.08 g of p-(trans-5-butyl-1,3-dioxan-2-yl)benzaldehyde in 30 ml of methylene chloride was added dropwise within 5 minutes. The mixture was subsequently stirred at 0° C. for a further 30 minutes, then the flask content was poured into 800 ml of hexane and the separated precipitate was filtered off (rinsing with hexane). The concentrated filtrate was digested with 400 ml of hexane, left to stand at 0° C. for 15 hours, filtered (rinsing with hexane) and the filtrate was concentrated. Low-pressure chromatography (0.5 bar) of the residue (8.2 g) on silica gel with hexane followed by petroleum ether/ethyl acetate/triethylamine (97:3:0.5) gave 3.23 g of trans-2-[p-(2,2-dibromovinyl)phenyl]-5-butyl-1,3-dioxane as colourless crystals (purity 95.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528114
Source datasetuspto-grants-1985_07
ORD IDord-182eff3c56b24314add3d8250cc33928
Source noteuspto-grants-1985_07