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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306503Generated: October 31, 2026

1,4-Dibromobenzene → HCID 70161136, compound

https://huagongshe.com/reaction/2306503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantHCID 14039070HCID 14039070—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 70161136HCID 7016113645.3%

Reaction Steps

A solution of 10.7 g of 1,4-dibromobenzene in 80 ml of absolute THF is cooled to −78° C. and treated within 30 min. with 25.6 ml of 1.6M butyllithium in hexane. After 30 min. 6.08 g of (4E,8E)-(RS)-4,8-dimethyl-10-(tetrahydro-pyran-2-yloxy)-deca4,8-dienal in 20 ml of THF are added dropwise. After 1 hr. at −78° C. the bath is removed until the suspension has dissolved and subsequently 7.2 ml of acetic acid in 10 ml of ether are added dropwise at −78° C. The solution is poured into saturated ammonium chloride solution/ethyl acetate. The organic phase is washed with saturated sodium bicarbonate solution and 10% sodium chloride solution, dried and evaporated. After silica gel chromatography with hexane/ethyl acetate 95:5 there are obtained 4.3 g of (4E,8E)-1-(4-bromo-phenyl)-4,8-dimethyl-10-(tetrahydro-pyran-2-yloxy)-deca-4,8-dien-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441177B1
Source datasetuspto-grants-2002_08
ORD IDord-78cca5ec8cde4492812ff2efbe427953
Source noteuspto-grants-2002_08