HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5959Generated: October 26, 2026
Methanol → 2-Benzoyloxy-4-hydroxymethylcyclobutanone
https://huagongshe.com/reaction/5959
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Benzoyloxy-3-hydroxymethyl-2-methylenecyclobutane | HCID 19794316 | — |
| Product | 2-Benzoyloxy-4-hydroxymethylcyclobutanone | HCID 19794318 | 86% |
Reaction Steps
A mixture of 2.09 g (9.5 mmol) of 1-benzoyloxy-3-hydroxymethyl-2-methylenecyclobutane from Step G, 112 mL of methylene chloride and 28 mL of methanol was cooled to -78° C. under a nitrogen atmosphere. Ozone was bubbled through the mixture for 10 minutes, until a persistent blue color was observed. Excess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide was added and the reaction mixture stirred for 0.5 h at -78° C. The reaction mixture was allowed to warm to ambient temperature, stirred for 0.5 h at ambient temperature and evaporated under reduced pressure to a syrup. The syrup (2.5 g) was dissolved to ~2 mL of methylene chloride and purified on a 1.5×45 cm silica gel column eluted @ 5 psi with 100 mL of methylene chloride, followed by 250 mL of 1% methanol in methylene chloride and 250 mL of 2% methanol in methylene chloride to give 1.79 g (86% yield) of the title compound; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246931 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-399011f1b64c4ac8aa1d59f797b46087 |
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| Source note | uspto-grants-1993_09 |
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