Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362296Generated: October 31, 2026

Malononitrile → HCID 53672594, compound

https://huagongshe.com/reaction/362296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54065816HCID 54065816—
SolventEthanolHCID 702—
ProductHCID 53672594HCID 53672594—

Reaction Conditions

Temperature65 °C

Reaction Steps

4.0 g of potassium tertiary butoxide are dissolved in 80 ml of ethanol and subsequently first 3.0 g of malononitrile and then 9 g of 2'-phenylamino-2-chloroacetophenone are added at RT and the mixture is stirred at 65° C. for 2 h. The mixture is then cooled and concentrated in an RE. The residue is partitioned between water and methylene chloride and the aqueous phase is extracted once more with methylene chloride. The combined organic phases are dried over MgSO4 and concentrated. The product is chromatographed on silica gel using methylene chloride and the product-containing fractions are concentrated, 4-(2-chlorophenyl)-1-phenyl-2-amino-3-cyanopyrrole being obtained as a reddish, viscous oil which is directly further processed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869485
Source datasetuspto-grants-1999_02
ORD IDord-f7f5f820dcd94c93b7d0659171a33966
Source noteuspto-grants-1999_02