HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890821Generated: October 29, 2026
3,4-dihydro-2H-pyran → HCID 66607810, compound
https://huagongshe.com/reaction/1890821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | HCID 178423521 | HCID 178423521 | — |
| Catalyst | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66607810 | HCID 66607810 | 98% |
Reaction Steps
3-(4-Bromo-3-methylphenyl)-4H-1,2,4-triazole (2.00 g, 8.40 mmol) was dissolved in tetrahydrofuran (10 mL) at room temperature with stirring under nitrogen. 3,4-Dihydro-2H-pyran (3.80 mL, 42.0 mmol) and methanesulfonic acid (0.027 mL, 0.42 mmol) were added and the resulting mixture heated at 50° C. under a reflux condenser under nitrogen for 20 h. The resulting mixture was cooled to room temperature, diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate and brine. The organics were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Flash chromatography (10-30-50% ethyl acetate in hexanes) gave the desired product (2.64 g, 8.22 mmol, 98% yield) as a yellow oil. MS (ESI) m/z 322 [M]+, 324 [M+2]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507492B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-ccdf2f6dfbd44ecb9973c7e1d4b68394 |
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| Source note | uspto-grants-2013_08 |
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