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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110850Generated: October 25, 2026

Methane → Prinomide Tromethamine

https://huagongshe.com/reaction/1110850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantPrinomideHCID 60352—
SolventEthanolHCID 702—
ProductPrinomide TromethamineHCID 3033812—

Reaction Steps

A suspension of 13.36 g of 1-methyl-beta-oxo-alpha-(phenylcarbamoyl)-2-pyrrolepropionitrile and 6.06 g of tromethamine in 100 ml of ethanol is heated to reflux for about one half hour, the solution is allowed to cool to about room temperature, treated with activated charcoal, filtered and reduced to a volume of about 45 ml at a temperature below 60°. The solution is heated to about 50°-55°, 100 ml of toluene is slowly added over a period of about one half hour with stirring and the resulting mixture is slowly cooled to about 15° over a period of one hour and stirred at 15° about 1 hour. The resulting crystalline product is collected by filtration, washed with toluene and dried at 70°-80° under low vacuum for 24 hours to yield 1-methyl-beta-oxo-alpha-(phenylcarbamoyl)-2-pyrrolepropionitrile tromethamine salt of Example 1. Second crop can be obtained by evaporating mother liquor to dryness and crystallizing more product from ethanol: toluene (1:2) as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977181
Source datasetuspto-grants-1990_12
ORD IDord-c01cb54ecc8b40ecade434d004ef137b
Source noteuspto-grants-1990_12