HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34828Generated: October 28, 2026
Sodium ethoxide → 5-[2-(2,2,2-Trifluoroethyl)guanidino]-3-hydroxymethyl-1,2,4-thiadiazole
https://huagongshe.com/reaction/34828
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Tetrahydropyranyloxyacetamidine hydrochloride | HCID 21298752 | — |
| Reactant | 3-(2,2,2-Trifluoroethyl)amino-5-amino-1,2,4-thiadiazole | HCID 21298777 | — |
| Product | 5-[2-(2,2,2-Trifluoroethyl)guanidino]-3-hydroxymethyl-1,2,4-thiadiazole | HCID 21298772 | — |
Reaction Steps
3-(2,2,2-Trifluoroethyl)amino-5-amino-1,2,4-thiadiazole (2.0 g.) and tetrahydropyranyloxyacetamidine hydrochloride (2.0 g.) was added to a solution of sodium ethoxide prepared from sodium (0.46 g.) and alcohol (50 ml.). The resulting mixture was stirred at 20° for 4 hours then heated under reflux for 60 hours. Volatile material was evaporated in vacuo and the residue was shaken with 2N hydrochloric acid (30 ml.) and ethyl acetate (30 ml.). The aqueous layer was further extracted with ethyl acetate (3×30 ml.) then the pH was adjusted to 10 with 2N sodium hydroxide. The basified mixture was extracted with ethyl acetate (6×30 ml.) and the combined extracts were dried (MgSO4) and evaporated in vacuo to give the crude product as an oil. It would be purified by fractionation on a silica gel column eluted with ethyl acetate to give 5-[2-(2,2,2-trifluoroethyl)guanidino]-3-hydroxymethyl-1,2,4-thiadiazole, m.p. 123°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762932 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-ae032892b3d34890992f8234ff336fbe |
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| Source note | uspto-grants-1988_08 |
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