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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863449Generated: October 30, 2026

1-Bromopropane → HCID 57489118, compound

https://huagongshe.com/reaction/1863449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesium HydroxideHCID 73981—
ReactantMagnesiumHCID 5462224—
ReactantHCID 20391526HCID 20391526—
ReactantHCID 178455851HCID 178455851—
SolventDiethyl EtherHCID 3283—
ProductHCID 57489118HCID 57489118—

Reaction Steps

A solution of 11.0 g of 1-(o-fluorobenzyl)-2-(dimethylaminoacetyl)pyrrole, free base of Example 3a, in ether is added dropwise to a stirring solution of n-propylmagnesium bromide which is prepared from 1.67 g of magnesium turnings and 8.4 g of n-propylbromide. The mixture is refluxed for 4 hours, allowed to cool, hydrolized with ice-water and treated with concentrated ammonium chloride solution to dissolve the magnesium hydroxide precipitate. The organic phase is separated and the aqueous phase extracted with ether and the organic phases are combined, washed with a 5% sodium bicarbonate solution and water and dried. Removal of the ether leaves a crude yellow oil which is distilled at 133°-137° C./0.08 mm gives a light yellow oil of 1-(dimethylamino)-2-[1-(o-fluorobenzyl)-2-pyrryl]-2-hydroxypentane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169095
Source datasetuspto-grants-1979_09
ORD IDord-05c21a560bc340a3ad581ecb13ba42e9
Source noteuspto-grants-1979_09