HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275996Generated: October 26, 2026
Acetic Acid → 2',5'-Dimethyl-4'-oxiranylacetanilide
https://huagongshe.com/reaction/275996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4'-(2-Bromoacetyl)-2',5'-dimethylacetanilide | HCID 22169659 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2',5'-Dimethyl-4'-oxiranylacetanilide | HCID 18316769 | 52.1% |
Reaction Steps
To a stirred solution of 4′-(2-bromoacetyl)-2′,5′-dimethylacetanilide (4.57 g) in ethanol (80 ml) was added sodium borohydride (608 mg) under ice-cooling, and the mixture was stirred for 1 hour. Acetic acid (3.7 ml) and water (200 ml) were added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in tetrahydrofuran (80 ml), and 5N aqueous sodium hydroxide solution (6.4 ml) was added to the solution under ice-cooling with stirring. The mixture was stirred for 30 minutes at room temperature, water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo. To the residue was added diethyl ether, and collection of the insoluble material by filtration gave 2′,5′-dimethyl-4′-oxiranylacetanilide (1.72 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353025B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-791e10e64421463a981458982202e6ee |
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| Source note | uspto-grants-2002_03 |
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