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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585592Generated: November 1, 2026

Ammonia → HCID 18424383, compound

https://huagongshe.com/reaction/1585592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium amideHCID 24533—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18424207HCID 18424207—
SolventDiethyl EtherHCID 3283—
ProductHCID 18424383HCID 18424383—

Reaction Steps

A solution of 6.68 g. (0.0219 mole) of ethyl 5-(p-chlorobenzoyl)-1-methylpyrrole-2-acetate in 50 ml. of ether is added to a solution of 0.94 g. (0.024 mole) of sodamide in about 150 ml. of liquid ammonia at -33° C. The mixture is allowed to reflux for 15 minutes and 3.10 g. (0.0219 mole) of methyl iodide is added. The mixture is stirred for one hour; then the ammonia is allowed to boil off. Ether and enough ammonium chloride to neutralize any anion are added. The mixture is poured into dilute hydrochloric acid and the ether solution is separated and washed with sodium bisulfite solution, sodium bicarbonate solution and brine. It is dried over anhydrous magnesium sulfate and evaporated to give an oily residue which crystallizes upon standing. The solid is recrystallized successively from cyclohexane and methanol to give a white crystalline solid, ethyl 5-(p-chlorobenzoyl)-α-methyl-1-methylpyrrole-2-acetate, m.p. 67-68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939417
Source datasetuspto-grants-1999_08
ORD IDord-efb928969caa436e926e97798b2d215b
Source noteuspto-grants-1999_08