HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541243Generated: October 26, 2026
Diethyl dithiophosphate, potassium salt → Methyl 5-carbamothioyl-2,4-dimethylbenzoate
https://huagongshe.com/reaction/541243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl dithiophosphate, potassium salt | HCID 1385274 | — |
| Reactant | Methyl 5-cyano-2,4-dimethylbenzoate | HCID 68288737 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | Methyl 5-carbamothioyl-2,4-dimethylbenzoate | HCID 86672528 | 57.1% |
Reaction Steps
To a round-bottom flask was added a solution of methyl 5-cyano-2,4-dimethylbenzoate (compound 2.3, 1.78 g, 9.41 mmol, 1.00 equiv) in tetrahydrofuran/H2O (30/3 mL). O,O′-diethyl dithiophosphate (3.30 g, 17.7 mmol, 2.00 equiv) was added and the resulting mixture was stirred for 2 days at 85° C. (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 extracted with 2×50 mL of ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:10) as eluent to furnish 1.20 g (57%) of the title compound as a 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-3b1ae739c03a4a65b263009a446ed7ef |
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| Source note | uspto-grants-2014_10 |
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