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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941000Generated: November 1, 2026

Tosylmethyl isocyanide → ethyl 4-(trifluoromethyl)-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/1941000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
ReactantEthyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Productethyl 4-(trifluoromethyl)-1H-pyrrole-3-carboxylateHCID 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-tolylsulfonylmethylisocyanide (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05702681
Source datasetuspto-grants-1997_12
ORD IDord-d5a51ae3a3b2402d83303d77b8ece831
Source noteuspto-grants-1997_12