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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282339Generated: October 29, 2026

Ammonia → HCID 18424383, compound

https://huagongshe.com/reaction/1282339

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 whch 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 numberUS06455703B2
Source datasetuspto-grants-2002_09
ORD IDord-c4221e4a156c4c3db5ba7c7dfa180d4a
Source noteuspto-grants-2002_09