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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589848Generated: October 30, 2026

Tosylmethyl isocyanide → HCID 66584156, compound

https://huagongshe.com/reaction/589848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
ReactantHCID 13415097HCID 13415097—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66584156HCID 6658415667.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 12.0 g (107 mmol) of potassium tert-butoxide at 60% in oil, in 100 ml of anhydrous tetrahydrofuran, is added dropwise a mixture of 13.3 g (71.1 mmol) of methyl (E)-3-(3-cyanophenyl)acrylate (CAS 193151-10-9) and 13.9 g (71.1 mmol) of tosylmethyl isocyanide (CAS 36635-61-7) dissolved in 100 ml of tetrahydrofuran, while maintaining the temperature of the reaction medium at about 25° C. The mixture is then stirred for 2 hours at room temperature, and is then partially concentrated under reduced pressure. This solution is then poured into ice-water and the reaction product is then extracted with dichloromethane. The organic phase is dried over sodium sulfate and the solvent is evaporated off under reduced pressure to give a brown solid, which is triturated in chloroform to give 10.8 g of methyl 4-(3-cyanophenyl)-1H-pyrrole-3-carboxylate in the form of a beige-coloured solid after cooling, filtering off and drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233965B2
Source datasetuspto-grants-2016_01
ORD IDord-97ae6d3274374d068a774c8e6ed0d369
Source noteuspto-grants-2016_01