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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372963Generated: October 25, 2026

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

https://huagongshe.com/reaction/372963

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°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162308
Source datasetuspto-grants-1992_11
ORD IDord-4895532cb52f432eb6f0a99c3b42bf1b
Source noteuspto-grants-1992_11