HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19746Generated: October 29, 2026
Epichlorohydrin → HCID 178513413, compound
https://huagongshe.com/reaction/19746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N'-hydroxy-3-(trifluoromethyl)benzimidamide | HCID 609330 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178513413 | HCID 178513413 | — |
Reaction Steps
50 g (0.245 mol) of m-trifluoromethyl-benzamidoxime and 33.7 g (0.6 mol) of potassium hydroxide was dissolved in a mixture of dimethyl sulphoxide and 170 ml of water, and the mixture was cooled to 0° C. 48 ml (0.6 mol) of epichlorohydrine was added, and the reaction mixture was stirred at 0° C. for 5 hours, then kept in a refrigerator overnight. Next day 250 ml of water was added, and the mixture was extracted with ethyl acetate (4×250 ml). The combined organic phases were washed with water, dried, treated with charcoal and evaporated to dryness, to yield m-trifluoromethyl-N-(2,3-epoxypropoxy)-benzamidine, as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745465B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1911c6d38c2143cabee43681d994bac6 |
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| Source note | uspto-grants-2010_06 |
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