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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493005Generated: October 30, 2026

Triethylamine → HCID 135407197, compound

https://huagongshe.com/reaction/1493005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantHCID 136403396HCID 136403396—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135407197HCID 13540719795.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxy-benzene carbothioic acid, hydrazide (2.0 g, 0.0072 mole) in tetrahydrofuran (10 ml) is added triethylamine (0.39 g, 0.0039 mole) followed by carbonyl diimidazole (0.8 g, 0.0048 mole). The resulting mixture is stirred at 0° C. for one hour. Dilute with ether and extract product with 1M NaOH (2×). The combined aqueous layers are combined and made acidic with aqueous 6M HCl. The product is extracted with 1:1 ether/ethyl acetate. The combined organic extracts are washed with saturated aqueous NaCl and concentration in vacuo provides 1.4 g (2.2 g theor., 64%) of 5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-1,3,4-thiadiazol-2(3H)-one after recrystallization from ethyl acetate/hexane: mp 229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05376670
Source datasetuspto-grants-1994_12
ORD IDord-5ba1886e7ccf4b448e5a7bec073adcab
Source noteuspto-grants-1994_12