HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222942Generated: November 1, 2026
Cesium carbonate → trans-N-cyanomethyl-2-(4-hydroxymethyl-phenylsulfanylmethyl)-cyclohexanecarboxamide
https://huagongshe.com/reaction/2222942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | (4-Triisopropylsilanylsulfanyl-phenyl)-methanol | HCID 69114972 | — |
| Reactant | trans-2-Bromomethyl-N-cyanomethylcyclohexanecarboxamide | HCID 86596125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | trans-N-cyanomethyl-2-(4-hydroxymethyl-phenylsulfanylmethyl)-cyclohexanecarboxamide | HCID 86596157 | — |
Reaction Steps
Cesium fluoride (0.829 g, 5.46 mmol) and cesium carbonate (0.456 g, 1.4 mmol) were added to a stirred solution of (4-triisopropylsilanylsulfanyl-phenyl)-methanol (0.808 g, 2.73 mmol) and trans-2-bromomethyl-cyclohexanecarboxylic acid cyanomethyl amide (0.906 g, 3.50 mmol) in dry dimethylformamide (910 mL). The reaction mixture was stirred at 50° C. overnight. The reaction mixture was diluted with dichloromethane and washed with 1N HCl, then with saturated aqueous sodium bicarbonate. The organic layer was dried with magnesium sulfate, filtered, and concentrated by rotary evaporation to yield trans-N-cyanomethyl-2-(4-hydroxymethyl-phenylsulfanylmethyl)-cyclohexanecarboxamide as a white solid that was carried forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371747B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-6b2a4f8837f44639bff10ff2221a7f90 |
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| Source note | uspto-grants-2008_05 |
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