HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735006Generated: October 30, 2026
3,4-dihydro-2H-pyran → HCID 178516157, compound
https://huagongshe.com/reaction/1735006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | HCID 178516162 | HCID 178516162 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178516157 | HCID 178516157 | 76.7% |
Reaction Steps
3-(Trifluoromethyl)-1H-pyrazol-5-ol (5.0 g, 0.032 mole) which is known in the art and p-toluene-sulfonic acid monohydrate (0.08 g) were dissolved in ethyl acetate (30 mL) and warmed to 50° C. 3,4-Dihydro-2H-pyran (2.9 g, 0.034 mole) was slowly added over a 10 minute period. After stirring 30 minutes at 50° C., the mixture was cooled and diluted with 100 mL of ethyl acetate. This solution was washed twice with 0.5% hydrochloric acid solution, then dried with magnesium sulfate, filtered and concentrated in vacuo. The residue was treated with 5 mL of ethyl acetate and 20 mL hexanes and filtered to give 1-(tetrahydro-2H-pyran-2-yl)-3-(trifluoromethyl)-1H-pyrazol-5-ol (5.8 g, 76% yield) as a white solid, mp=129°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05536701 |
|---|
| Source dataset | uspto-grants-1996_07 |
|---|
| ORD ID | ord-7300d717b2174532926c5ad7058295d7 |
|---|
| Source note | uspto-grants-1996_07 |
|---|