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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541301Generated: October 30, 2026

Tetrahydrofuran → Methyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoate

https://huagongshe.com/reaction/541301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiethyl dithiophosphate, potassium saltHCID 1385274—
ReactantMethyl 5-cyano-4-cyclobutyl-2-ethylbenzoateHCID 68288744—
SolventWaterHCID 962—
ProductMethyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoateHCID 8667253238.1%

Reaction Steps

To a round-bottom flask was added a solution of methyl 5-cyano-4-cyclobutyl-2-ethylbenzoate (compound 181.5, 3.00 g, 12.3 mmol, 1.00 equiv) in a solvent mixture of tetrahydrofuran and H2O (80 mL/40 mL). To this was added O,O′-diethyl dithiophosphate (6.69 g, 35.9 mmol, 3.00 equiv) dropwise with stirring. The resulting solution was stiffed at 85° C. for 48 h (CAUTION: significant gas evolution occurs—this and all other reactions described herein should be carried out in well ventilated fume hoods). After cooling to ambient temperature, the mixture was then concentrated in vacuo. The crude product was purified by re-crystallization from petroleum ether to furnish 1.30 g (38%) of methyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-4262186ea80b404c89eba126a2134b40
Source noteuspto-grants-2014_10