HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629993Generated: October 30, 2026
Tosylmethyl isocyanide → HCID 66584156, compound
https://huagongshe.com/reaction/1629993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | HCID 13415097 | HCID 13415097 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66584156 | HCID 66584156 | 67.1% |
Reaction Steps
To a suspension of 12.0 g (107 mmol) of potassium tert-butoxide at 60% in oil, in 100 ml of anhydrous tetrahydrofuran, is added dropwise a mixture of 13.3 g (71.1 mmol) of methyl(E)-3-(3-cyanophenyl)acrylate (CAS 193151-10-9) and 13.9 g (71.1 mmol) of tosylmethyl isocyanide (CAS 36635-61-7) dissolved in 100 ml of tetrahydrofuran, while maintaining the temperature of the reaction medium at about 25° C. The mixture is then stirred for 2 hours at room temperature, and is then partially concentrated under reduced pressure. This solution is then poured into ice-water and the reaction product is then extracted with dichloromethane. The organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure to give a brown solid, which is triturated in chloroform to give 10.8 g of methyl 4-(3-cyanophenyl)-1H-pyrrole-3-carboxylate in the form of a beige-coloured solid after cooling, filtering off and drying.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791119B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-288cdce0cf9743a6907c2d3e8f9b60c6 |
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| Source note | uspto-grants-2014_07 |
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