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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494261Generated: October 30, 2026

1,6-Dibromohexane → 1-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene

https://huagongshe.com/reaction/1494261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantHCID 12950402HCID 12950402—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzeneHCID 1498644115%

Reaction Steps

To 27.0 g (0.139 mole) of 1,2-dimethoxy-3-(1,1-dimethylethyl)benzene in 350 mL of anhydrous tetrahydrofuran cooled in an ice-brine bath at -5° was added. 87 mL (0.139 mole) of 1.6M butyl lithium in hexane over 30 minutes. The reaction mixture was stirred at -5° for 3 hours and then at reflux for 1 hour. After cooling in an ice bath, 21.5 mL (0.139 mole) of 1,6-dibromohexane in 75 mL of tetrahydrofuran was added dropwise. The reaction mixture was then stirred at reflux for 17 hours. The solvent was removed under reduced pressure, 50 mL of 3N hydrochloric acid was added and the product was extracted with ether. The extract was washed with sodium bicarbonate solution, dried and concentrated at reduced pressure to an oil. Purification by HPLC using 20% toluene-hexane gave 7.6 g ((15% yield) of 1-(6-bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025036
Source datasetuspto-grants-1991_06
ORD IDord-c374b92fbf8045c0b99ec29fd43025a0
Source noteuspto-grants-1991_06