HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589880Generated: October 30, 2026
Tosylmethyl isocyanide → HCID 66584760, compound
https://huagongshe.com/reaction/589880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | HCID 5373048 | HCID 5373048 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66584760 | HCID 66584760 | 61.4% |
Reaction Steps
To a suspension of 38.3 g (341 mmol) of potassium tert-butoxide at 60% in oil in 500 ml of anhydrous tetrahydrofuran is added dropwise a mixture of 55.2 g (284 mmol) of ethyl (E)-3-(3-fluorophenyl)acrylate (CAS 166250-00-6) and 55.5 g (284 mmol) of tosylmethyl isocyanide (CAS 36635-61-7) dissolved in 500 ml of tetrahydrofuran, while maintaining the temperature of the reaction medium at about 25° C. The mixture is then stirred for 1 hour 30 minutes at room temperature. The mixture is then poured into saturated aqueous solution and the reaction product is extracted with ethyl acetate. The organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure, to give a brown solid, which is chromatographed on a column of silica gel, eluting with dichloromethane, to give 40.7 g of ethyl 4-(3-fluorophenyl)-1H-pyrrole-3-carboxylate, in the form of a white powder after triturating in diisopropyl ether, filtering off and drying.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09233965B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-ec65bc5b1a87482a826275519caef694 |
|---|
| Source note | uspto-grants-2016_01 |
|---|