Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 67794438 | HCID 67794438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19982294 | HCID 19982294 | 43.3% |
Reaction Steps
Oxone was bubbled through a solution of 3,4,5-triphenyl-lH-pyrazole-1-undecene (6.78 g, 15 mmol) in dichloromethane (175 mL) and methanol (0.73 g, 22 mmol) maintained at -78° C. for 1.5 hours. The ozone supply was removed, dimethylsulfide (30 mL) added and the mixture allowed to warm to room temperature over 2 hours. The solution was dried over sodium sulfate, concentrated in vacuo and the residue chromatographed on a column of silica gel. Elution with a mixture of hexane and ethyl acetate (9:1) gave 3,4,5-triphenyl-lH-pyrazole-1-decanal (2.93 g, 43%) as an oil. MS(CI): m/e =451 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994482 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-a457c9712fd64c68aa2c8a8448c947b5 |
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| Source note | uspto-grants-1991_02 |
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