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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581781Generated: November 2, 2026

Ethyl orthoformate → HCID 135744212, compound

https://huagongshe.com/reaction/1581781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant4-chloro-2-hydroxybenzohydrazideHCID 4996481—
ProductHCID 135744212HCID 13574421235%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 4-chloro-2-hydroxybenzoic acid hydrazide (Chemical Abstracts, 93:7808, 475 mg, 2.55 mmol) and triethylorthoformate. (3.6 ml) is heated at 130° C. for 3.5 hours. After cooling, a precipitate formed and is collected by filtration. The filter cake is recrystallized from methanol to give 173 mg (35%) of 5-chloro-2-(1,3,4-oxadiazol-2-yl)phenol. This phenolic product is reacted with (2S)-glycidyl 3-nitrobenzenesulfonate substantially as described for Epoxide 1 to yield 170 mg (69%) of the title epoxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730792B2
Source datasetuspto-grants-2004_05
ORD IDord-d88f3995ee7a4feb9258937e4e340117
Source noteuspto-grants-2004_05