Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604705Generated: November 1, 2026

Hexane → HCID 46205463, compound

https://huagongshe.com/reaction/604705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-BromophenetoleHCID 68523—
Reactant3-BromobenzaldehydeHCID 76583—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46205463HCID 4620546390%

Reaction Steps

A 2.6 M n-butylithium hexane solution (5.8 mL) was added to a mixture of 4-bromophenetole (2.87 g, 0.0143 mol) and tetrahydrofuran (30 mL) at −78° C. After the mixture was stirred for 0.5 hours, a tetrahydrofuran (15 mL) solution of 3-bromobenzaldehyde (2.65 g, 0.0143 mol) was added, and further stirred for 15 minutes to warm the reaction mixture to room temperature. After the reaction mixture was added with a saturated ammonium chloride aqueous solution and extracted with ethyl acetate, the organic layer was washed with brine and dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=7:1 to 5:1) to obtain colorless oily (3-bromophenyl)(4-ethoxyphenyl)methanol (3.94 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910619B2
Source datasetuspto-grants-2011_03
ORD IDord-8754515a13454143a3354f6e8d0ebed6
Source noteuspto-grants-2011_03