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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-1-(4-chlorophenyl)ethan-1-ol | HCID 236800 | — |
| Reactant | 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran | HCID 13071284 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | Phosphorus oxychloride | HCID 24813 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | trans-6-(2,4-Dichlorophenoxymethyl)-2-[2-bromo-1-(4-chlorophenyl)ethoxy]tetrahydropyran | HCID 53718043 | 30.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04421758 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-cdf87a7c11d84c979c5af835a820cb6a |
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| Source note | uspto-grants-1983_12 |
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