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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651297Generated: November 1, 2026

Formic Acid → 3H-1,2,4-Triazol-3-one

https://huagongshe.com/reaction/1651297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
ReactantSemicarbazideHCID 5196—
ProductSemicarbazideHCID 5196—
Product3H-1,2,4-Triazol-3-oneHCID 1107333947.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

Aqueous semicarbazide free base feedstock (523.8 grams) was prepared from 64 percent N2H4 (4.18 moles) and urea (4.17 moles) by the method of Example 1. Thirty-seven percent hydrochloric acid (205.6 grams, 2.08 moles) and 90 percent formic acid (533.3 grams, 10.44 moles) were successively added to the aqueous semicarbazide free base. The mixture was heated to 107°-110° C. for four hours; a formic acid-H2O azeotrope distilled (610.5 grams), followed by H2O addition (160 ml) and resumption of stripping (107 grams). After cooling to 10° C., the mother liquor was siphoned (307 grams). The crude 1,2,4-triazol-5-one was recrystallized from H2O (760 ml). After cooling to 10° C., the supernatant liquid was siphoned (807 grams) and the product was slurried with an additional 210 ml H2O (10° C.), filtered, and vacuum-dried to give 168.5 grams of 1,2,4-triazol-5-one (1.98 moles, 47.4 percent yield based on N2H4 charged), m.p. 236.5°-8° C. (Cl-, 0.22 percent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927940
Source datasetuspto-grants-1990_05
ORD IDord-9d460c020b874f4aae71b8e7d03fc609
Source noteuspto-grants-1990_05