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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073472Generated: October 30, 2026

Ammonium Chloride → HCID 14391477, compound

https://huagongshe.com/reaction/2073472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 11959626HCID 11959626—
ReactantHCID 14391470HCID 14391470—
Catalyst1,1-DibromoethaneHCID 11201—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14391477HCID 1439147751.9%

Reaction Steps

To a suspension of magnesium turnings (1.0 g, 0.04 mole) in 25 ml tetrahydrofuran (THF) and 10 ml ether, was added a few drops of a solution of 2-bromo-1-(2-fluorobenzyl) pyrrole (10.0 g, 0.04 mole) in 30 ml THF. The reaction was initiated with a few drops of dibromoethane and heat, and reflux was maintained by the addition of the bromo compound after stirring at reflux for 30 minutes, the mixture was cooled with an ice-bath; then a solution of 1-(4-chlorophenethyl)-4-piperidone (5.0 g, 0.021 mole) was added. After stirring at ambient temperature for one hour, the mixture was poured into a solution of NH4Cl, then extracted with ether. The ether solution was washed with water, then dried over anhydrous MgSO4. After evaporation of the solvent, the resultant oil, 12 g, was purified by high pressure liquid chromatography (HPLC), using ethyl acetate as the eluent to give 4.5 g of 1-(4-chlorophenethyl)-4-[1-(2 -fluorobenzyl) pyrrol-2-yl]-4-piperidinol, m.p. 108°-9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918069
Source datasetuspto-grants-1990_04
ORD IDord-543854546b88449cacda81c4104aa967
Source noteuspto-grants-1990_04