Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630023Generated: November 2, 2026

Tosylmethyl isocyanide → HCID 66584760, compound

https://huagongshe.com/reaction/1630023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
ReactantHCID 5373048HCID 5373048—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66584760HCID 6658476061.4%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791119B2
Source datasetuspto-grants-2014_07
ORD IDord-5c0bc25f5638410e9881ab84f9393d32
Source noteuspto-grants-2014_07