HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093155Generated: October 26, 2026
Triethylamine hydrochloride → Methyl 4-carbamothioyl-3-methylbenzoate
https://huagongshe.com/reaction/2093155
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Methyl 4-cyano-3-methylbenzoate | HCID 19969932 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 4-carbamothioyl-3-methylbenzoate | HCID 53832239 | — |
Reaction Steps
To a solution of methyl 4-cyano-3-methylbenzoate (36 mg, 0.205 mmol) in 1,4-dioxane (0.5 mL) and water (0.500 mL), was added sodium hydrogen sulfide (0.019 mL, 0.616 mmol) and triethylamine hydrochloride (170 mg, 1.233 mmol). The reaction mixture was heated at 55° C. overnight. The reaction was allowed to cool and water was added. The mixture was extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and the solvent was evaporated in vacuo to give the product as a yellow solid. LCMS calc.=210.1; found=210.2 (M+1)+. 1H NMR (500 MHz, CDCl3) 7.86 (s, 1 H); 7.84 (d, J=8.1 Hz, 1 H); 7.42 (d, J=7.9 Hz, 1 H); 7.16 (s, 2 H); 3.93 (s, 3 H); 2.51 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440702B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-3991a109155b4e399845a93c6e86aa2f |
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| Source note | uspto-grants-2013_05 |
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