HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167707Generated: October 27, 2026
Phosphate → 2-(3,4-Difluorophenyl)-2-methyloxirane
https://huagongshe.com/reaction/1167707
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1,2-Difluoro-4-(prop-1-en-2-yl)benzene | HCID 15525212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3,4-Difluorophenyl)-2-methyloxirane | HCID 22993508 | — |
Reaction Steps
To a biphasic solution of 1,2-difluoro-4-isopropenyl-benzene (0.81 g, 5.1 mmol) in CH2Cl2 (50 mL) and 50 mL of phosphate buffer (made by dissolving 0.3 g of NaHPO4 and 0.35 g of NaH2PO4 in 50 mL water, pH=8) at 0° C., was added a solution of 3-chloroperoxybenzoic acid (approx. 75% solid, 3.32 g, 10.2 mmol) via a dropping funnel fitted with a cotton plug dropwise in two batches. The solution was stirred at room temperature overnight. It was extracted with CH2Cl2, washed with sat. Na2S2O4 solution followed by water. The organic layer was finally washed with sat. NaHCO3, separated, dried over Na2SO4, filtered and solvent was removed in vacuo. 2-(3,4-Difluorophenyl)-2-methyl-oxirane was obtained as a pale yellow oil (0.65 g, 74% yield). It was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620815B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-72d06748f3314ff49732401631fe4396 |
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| Source note | uspto-grants-2003_09 |
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