HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran → HCID 54156467, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran | HCID 13071284 | — |
| Reactant | 2-Bromo-1-(2,4-dichlorophenyl)ethanol | HCID 13386071 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | Phosphorus oxychloride | HCID 24813 | — |
| Product | HCID 54156467 | HCID 54156467 | — |
Reaction Steps
To 10 ml of an ethereal solution of 425 mg of α-bromomethyl-2,4-dichlorobenzyl alcohol and 340 mg of 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran was added a catalytic amount (2 drops) of phosphorus oxytrichloride, and the mixture was stirred at room temperature for 4 days. 3 drops of triethylamine were then added and the solvent was evaporated off under reduced pressure. The residue was purified by column chromatography through silica gel eluted with a 40:2:1 by volume mixture of hexane, benzene and ethyl acetate, to give 681 mg of the isomer of lesser polarity of trans-6-(2,4-dichlorophenoxymethyl)-2-[2-bromo-1-(2,4-dichlorophenyl)ethoxy]tetrahydropyran as colorless crystals melting at 104°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04421758 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-6af0ef801ada4a85967df643069c150f |
| Source note | uspto-grants-1983_12 |