HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989131Generated: November 2, 2026
3,4-dihydro-2H-pyran → 2-Bromo-6-(tetrahydro-pyran-2-yloxymethyl)-4-(4-trifluoromethyl-phenyl)-pyridine
https://huagongshe.com/reaction/1989131
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Reactant | [6-Bromo-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-methanol | HCID 60209333 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-6-(tetrahydro-pyran-2-yloxymethyl)-4-(4-trifluoromethyl-phenyl)-pyridine | HCID 57468698 | 87.2% |
Reaction Steps
To a solution of the above described [6-bromo-4-(4-trifluoromethyl-phenyl)-pyridin-2-yl]-methanol (4.2 g, 95%, purity 81%) and 3,4-dihydro-2H-pyran (1.4 ml, 15.4 mmol) in DCM (20 ml) at 23° C. was added a catalytic amount of p-TsOH.H2O (10 mg) and the mixture was stirred at 23° C. for 18 h. Then again 3,4-dihydro-2H-pyran (0.7 ml, 7.68 mmol) was added and stirring was continued at 23° C. for another 2 h. The entire reaction mixture was directly subjected to silica gel column chromatography with n-heptane/AcOEt to give the title compound (4.59 g, 100%, 93% purity) as a light yellow oil. MS (ISP) 418.2 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642264B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-770d8dd8f9274c1b9630043dbe579e66 |
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| Source note | uspto-grants-2010_01 |
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