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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460646Generated: November 1, 2026

Diethyl Ether → (R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromide

https://huagongshe.com/reaction/1460646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantThionyl bromideHCID 68176—
Reactant(R)-1-(2-hydroxyethyl)nipecotic acid ethyl esterHCID 54103225—
SolventTolueneHCID 1140—
Product(R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromideHCID 70009171131.7%

Reaction Steps

A sample of the above alcohol (140 g, 0.70 mole) was dissolved in toluene (400 ml) and thionyl bromide (80 ml, 0.77 mole) was introduced with vigorous stirring. After 1.5 h the exotherm reaction had subsided and diethyl ether (400 ml) was added. The resultant precipitate was collected by filtration and washed with diethyl ether. The solid was triturated with ethyl acetate, again collected on a filter and dried to provide (R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromide (175 g, 73%) as a white solid, m.p. 210°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071859
Source datasetuspto-grants-1991_12
ORD IDord-8ce19c628e5543d1b2efa1e3a974c5e7
Source noteuspto-grants-1991_12