HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584152Generated: October 26, 2026
m-Chloroperbenzoic acid → 2,3-Epoxy-[4-(tert-butoxycarbonyl)phenoxy]butane
https://huagongshe.com/reaction/584152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | trans-4-[4-(Tert-butoxycarbonyl)phenoxy]-2-butene | HCID 22345517 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Epoxy-[4-(tert-butoxycarbonyl)phenoxy]butane | HCID 22345537 | 96% |
Reaction Steps
A solution of trans-4-[4-(tert-butoxycarbonyl)phenoxy]-2-butene (3.10 g, 12.48 mmol) in dry dichloromethane (50 ml) was treated at 22° C. with 3-chloroperoxybenzoic acid (4.30 g, 24.9 mmol) and the resulting mixture was stirred at 22° C. for 18 hours. The mixture was then diluted with toluene, washed with 5% sodium thiosulfate, saturated sodium bicarbonate and brine. After drying (sodium sulfate), evaporation of the solvent gave an oil that was chromatographed on silica gel. Elution with a mixture of toluene and ethyl acetate (95:5) gave 3.16 g (96%) of the title material as an oil which solidified upon standing: bp 85-90° C./0.05 torr (bulb to bulb, air bath temperature); mp 47-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924391B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-d67d261053a94aff9cf5845ffc441e9f |
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| Source note | uspto-grants-2005_08 |
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