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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029535Generated: November 1, 2026

Ethyl Acetate → HCID 4397989, compound

https://huagongshe.com/reaction/1029535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantThiophosgeneHCID 10040—
Reactant3,5-Di-tert-butyl-4-hydroxyhydrocinnamic acid hydrazideHCID 64865—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
ProductHCID 4397989HCID 439798916%

Reaction Steps

Thiophosgene (0.55 mL, 6.80 mmol) is added dropwise to a -78° C. solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid hydrazide (2.0 g, 6.8 mmol) in tetrahydrofuran (200 mL). The reaction mixture is stirred for 10 minutes then poured into a separatory funnel containing ethyl acetate and aqueous sodium bicarbonate. The organic phase is washed three times with water and once with brine. Drying the organic phase over magnesium sulfate and evaporation gives a heavy oil which is crystallized from ethyl acetate/hexane. The product is chromatographed on a column of silica with ethyl acetate/dichloromethane (5/95) and recrystallized from dichloromethane/hexane to afford 0.36 g (16%) of 5-[2-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]ethyl]-1,3,4-oxadiazole-2(3H)-thione, mp 164.5°-165.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102897
Source datasetuspto-grants-1992_04
ORD IDord-060fe457371645a99232a6173ff849ba
Source noteuspto-grants-1992_04