HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827518Generated: November 3, 2026
3,4-dihydro-2H-pyran → HCID 22137302, compound
https://huagongshe.com/reaction/1827518
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 4-Hydroxy-3-methylbenzaldehyde | HCID 139901 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22137302 | HCID 22137302 | 89.6% |
Reaction Steps
To a solution of 4-hydroxy-3-methylbenzaldehyde (3.0 g, 22.03 mmol) in 45 mL methylene chloride was added 3,4-dihydro-2H-pyran (5.0 mL, 54.8 mmol) and pyridinium p-toluenesulfonate (0.55 g, 2.19 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was partitioned between methylene chloride and saturated aqueous sodium bicarbonate. The layers were separated and the aqueous layer was extracted with three portions of methylene chloride. The combined organic layers were washed with saturated aqueous sodium chloride, dried (sodium sulfate), filtered, and concentrated. Silica gel flash chromatography of the residue (10% ether/hexanes to 20% ether/hexanes) afforded 4.35 g of the title compound of Step A. MS 221.1 (M+1)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053212B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-4e15f7a7a76842ba8dc3ddb5b850502b |
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| Source note | uspto-grants-2006_05 |
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