Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456622Generated: October 31, 2026

1H-1,2,4-Triazole → HCID 54136983, compound

https://huagongshe.com/reaction/1456622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 54262066HCID 54262066—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54136983HCID 54136983—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of the compound prepared as described in Example 4 (318 mg), triphenylphosphine (577 mg), and 1,2,4-triazole (152 mg) in dry tetrahydrofuran (4.5 ml) was cooled to about 5° C., and treated with diethyl azodicarboxylate (383 mg) over a ten minute period. After the addition was complete, the reaction was allowed to warm to room temperature. After about 17 hours, the reaction solution was concentrated in vacuo and allowed to stand at room temperature under reduced pressure to give a crystalline solid. This solid was diluted with chloroform and purified by centrifugal thin-layer chromatography, eluting with ethyl acetate/hexane (1:1) followed by ethyl acetate/hexane (3:1), ethyl acetate, ethyl acetate/methanol (19:1), and ethyl acetate/methanol (9:1). The fractions containing the title compound were combined and concentrated in vacuo to give 280 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843997
Source datasetuspto-grants-1998_12
ORD IDord-8b0bea0189b5479889fb75fb2b936822
Source noteuspto-grants-1998_12