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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905070Generated: October 25, 2026

2-Bromo-1-(4-chlorophenyl)ethan-1-ol → trans-6-(2,4-Dichlorophenoxymethyl)-2-[2-bromo-1-(4-chlorophenyl)ethoxy]tetrahydropyran

https://huagongshe.com/reaction/905070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(4-chlorophenyl)ethan-1-olHCID 236800—
Reactant2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyranHCID 13071284—
CatalystTriethylamineHCID 8471—
CatalystPhosphorus oxychlorideHCID 24813—
SolventDiethyl EtherHCID 3283—
Producttrans-6-(2,4-Dichlorophenoxymethyl)-2-[2-bromo-1-(4-chlorophenyl)ethoxy]tetrahydropyranHCID 5371804330.3%

Reaction Steps

To a solution of 259 mg of α-bromomethyl-4-chlorobenzyl alcohol and 311 mg of 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran in 6 ml of diethyl ether was added one drop of phosphorus oxytrichloride, and the mixture was stirred at room temperature for 1 day. After 3 drops of triethylamine had been added, the solvent was evaporated off under reduced pressure and the residue was purified by column chromatography through silica gel eluted with a 5:50:11 by volume mixture of benzene, hexane and ethyl acetate, to give 147 mg of the isomer of lesser polarity of trans-6-(2,4-dichlorophenoxymethyl)-2-[2-bromo-1-(4-chlorophenyl)ethoxy]tetrahydropyran melting at 86°-87° C., 165 mg of the isomer of greater polarity melting at 97°-98° C., and 80 mg of a mixture thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04421758
Source datasetuspto-grants-1983_12
ORD IDord-cdf87a7c11d84c979c5af835a820cb6a
Source noteuspto-grants-1983_12