HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292598Generated: October 31, 2026
Toluene → 2-Methylcyclohexyl 2-chloro-5[(phenylthiomethyl)amino]benzoate
https://huagongshe.com/reaction/1292598
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methylcyclohexyl 2-chloro-5-(benzoylamino)benzoate | HCID 18915807 | — |
| Product | 2-Methylcyclohexyl 2-chloro-5[(phenylthiomethyl)amino]benzoate | HCID 18915806 | — |
Reaction Steps
To a solution of 2-methylcyclohexyl 2-chloro-5-(benzoylamino)benzoate (1.8 g, 0.0048 mole) in toluene (100 ml) was added Lawesson's Reagent (2.5 g), sodium bicarbonate (1.0 g) to produce the reaction mixture. The reaction mixture was stirred and refluxed for 4 hours. The reaction mixture was then cooled to ambient temperature which resulted in the formation of a white solid precipitate. The white solid was filtered off. The filtrate was then passed through a short column of aluminum oxide (neutral) using ether/hexane as eluent to give a yellow solution. The yellow solution was concentrated and a yellow solid crystallized. The yellow solid was filtered to give 2-methylcyclohexyl 2-chloro-5[(phenylthiomethyl)amino]benzoate as a yellow solid (1.3 g, m.p. 143°-144° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756813 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-31d5a0b6619c44e6b0fd7fd759580367 |
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| Source note | uspto-grants-1998_05 |
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