HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227106Generated: October 31, 2026
3,4-dihydro-2H-pyran → 1-(4'-(2-Tetrahydropyranyloxy)phenyl)-3-bromopropane
https://huagongshe.com/reaction/2227106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(3-Bromopropyl)phenol | HCID 14817036 | — |
| Catalyst | Phosphorus oxychloride | HCID 24813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4'-(2-Tetrahydropyranyloxy)phenyl)-3-bromopropane | HCID 18471790 | — |
Reaction Steps
To a solution of 1-(4′-hydroxyphenyl)-3-bromopropane 3B (3.56 g) in dichloromethane (11 mL) is added dihydropyran (2.3 mL). The reaction mixture is cooled to 0° C., and three drops of phosphorus oxychloride are added. The reaction mixture is stirred in the ice bath for a further two hours, then gradually allowed to warm to room temperature, where it is allowed to stir overnight. To the reaction mixture is then added potassium carbonate (3 g), and the reaction mixture is stirred an additional hour. The solid is then filtered out, and the solvents and residual DHP is removed in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413448B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-3936bb0374a549fba4004c4ecbb16f12 |
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| Source note | uspto-grants-2002_07 |
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