HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tosylmethyl isocyanide → ethyl 4-(trifluoromethyl)-1H-pyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | Ethyl (2E)-4,4,4-trifluoro-2-butenoate | HCID 5371261 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 4-(trifluoromethyl)-1H-pyrrole-3-carboxylate | HCID 14370786 | — |
Reaction Conditions
| Temperature | -60 °C |
|---|
Reaction Steps
A solution of potassium t-butoxide (8.11 g, 0.075 mol) in tetrahydrofuran at -60° C. is treated dropwise with a mixture of ethyl 4,4,4-trifluorocrotonate (10.5 g, 0.063 mol) and p-tolylsulfonyl-methylisocyanide (12.2 g, 0.063 mol) in tetrahydrofuran over a 1 hour period, stirred at -60° C. for 30 minutes, allowed to warm to room temperature and quenched with water. The reaction mixture is extracted with ether and ethyl acetate. The combined extracts are washed with brine, dried (MgSO4) and concentrated in vacuo to give a solid residue. Recrystallization from 1,2-dichloroethane affords the title compound as a tan solid, 7.3 g (56%), mp 163° to 164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371239 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-ad8b640e75524157b86dee8d332c4e03 |
| Source note | uspto-grants-1994_12 |