HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883093Generated: November 1, 2026
Water → 4'-Tetrahydropyranyloxy-acetophenone
https://huagongshe.com/reaction/1883093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4'-Tetrahydropyranyloxy-acetophenone | HCID 11390381 | 62% |
Reaction Steps
13.62 g (100 mmol) of 4-hydroxyacetophenone and 10.04 ml (110 mmol) of 3,4-dihydro-2H-pyran were suspended in 100 ml of anhydrous methylene chloride. At 0° C., 190 mg (1 mmol) of p-toluenesulfonic acid were added with stirring and the mixture was stirred at 0° C. for 3 hours. 10.04 ml (110 mmol) of 3,4-dihydro-2H-pyran were added again and the mixture was stirred at room temperature for a further 3 hours. The batch was poured into 150 ml of water, the phases were separated and the organic phase was extracted with saturated NaHCO3 solution, saturated NaCl solution and with water. The organic phase was dried over sodium sulfate, concentrated and, for purification, chromatographed on silica gel (70-200 μm) using methylene chloride as an eluent. 13.65 g (62%) of 10.1 were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759424B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-a388cc93a8014e02a187ea41243dd532 |
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| Source note | uspto-grants-2004_07 |
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