HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4146Generated: October 29, 2026
Peracetic Acid → 4-(2,3-Epoxypropyl)-2,6-dimethylphenyl glycidyl ether
https://huagongshe.com/reaction/4146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Allyl-2,6-dimethylphenyl glycidyl ether | HCID 19836221 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2,3-Epoxypropyl)-2,6-dimethylphenyl glycidyl ether | HCID 20152704 | 863.5% |
Reaction Steps
A 350 ml sulfurating flask equipped with thermometer, stirrer, cooler and drip funnel is charged with 46.30 g (0.21 mole) of 4-allyl-2,6-dimethylphenyl glycidyl ether, 1.93 g of sodium acetate and 160 ml of chloroform, and the batch is heated to 35°-40° C. At this temperature, 52.3 g (0.28 mole) of 40% peracetic acid are then added dropwise over about 1 hour. The reaction mixture is then held at this temperature for a further 4 hours until the educt is no longer discernible in the gas chromatograph. When the reaction is complete, the reaction mixture is diluted in chloroform and the resultant solution is washed with 3% NaOH until neutral, made peroxide-free with sodium sulfite, dried over sodium sulfate and filtered. The filtrate is concentrated by rotary evaporation, affording 47.6 g of 4-(2,3-epoxypropyl)-2,6-dimethylphenyl glycidyl ether in the form of a low viscous oil; epoxide content 8.1 equivalents/kg (95.13% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04724031 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-d41592ac9b864e5fa8d5045e4e4bc7fb |
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| Source note | uspto-grants-1988_02 |
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