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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088706Generated: November 2, 2026

Dichloromethane → 2-[2-[(6-Bromohexyl)oxy]ethyl]quinoline

https://huagongshe.com/reaction/1088706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
Reactant2-QuinolineethanolHCID 70532—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-[2-[(6-Bromohexyl)oxy]ethyl]quinolineHCID 22161749—

Reaction Steps

A mixture of 2-quinolineethanol (1.00 g), 1,6-dibromohexane (4 ml), TAB (100 mg), 50% aqueous sodium hydroxide (4 ml) and dichloromethane (3 ml) was stirred at room temperature for 40 h, then diluted with water (40 ml) and ether (25 ml). The organic phase was washed with water (20 ml), dried and evaporated in vacuo. The residual oil was purified by FCC eluting with hexane followed by hexane-ether (9:1) and ether, to give the title compound (1.18 g) as a pale yellow oil, t.l.c. (diethyl ether) Rf 0.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963564
Source datasetuspto-grants-1990_10
ORD IDord-7431bd3e640a4eb8959f2b7909f12814
Source noteuspto-grants-1990_10