HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72313Generated: October 24, 2026
Propargyl alcohol → [3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanol
https://huagongshe.com/en/reaction/72313
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | 4-Benzyloxy-benzaldehyde oxime | HCID 763359 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanol | HCID 64164588 | — |
Reaction Steps
4-benzyloxy-benzaldehyde oxime (2.27 g, 10 mmol-a compound of 92% purity) was dissolved in methylene chloride (40 ml, 0.25 M), to which solution was added propargyl alcohol (1.77 ml, 30 mmol). To the resulting solution was very slowly dropwise added 10% NaOCl (13.7 ml, 20 mmol) at 0° C., using a dropping funnel. After the addition of NaOCl was completed, the mixture was stirred for about 5 hours while increasing the temperature slowly to room temperature. The completion of the reaction was confirmed by liquid chromatography, and the mixture was distilled under reduced pressure to remove the methylene chloride. Water (200 ml) was added to the residue and the resulting solid was filtered off. The filtered compound was washed with excess of water and finally washed with diethyl ether. The thus-obtained solid compound was recrystallized from ethyl acetate/hexane (1:2) to obtain 2.50 g of [3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-methanol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828992B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5fbbabaf954345bd939643f966166217 |
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| Source note | uspto-grants-2014_09 |
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