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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diethyl dithiophosphate, potassium salt | HCID 1385274 | — |
| Reactant | Methyl 5-cyano-4-cyclobutyl-2-ethylbenzoate | HCID 68288744 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-carbamothioyl-4-cyclobutyl-2-ethylbenzoate | HCID 86672532 | 38.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871790B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4262186ea80b404c89eba126a2134b40 |
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| Source note | uspto-grants-2014_10 |
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