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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381167Generated: November 2, 2026

1-Bromo-3-methoxypropane → HCID 66788050, compound

https://huagongshe.com/reaction/2381167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methoxypropaneHCID 524551—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66788050HCID 66788050—

Reaction Steps

To a pre-cooled THF solution (200 ml) under an argon atmosphere was added at −5° C. LDA (2M in THF/heptane/ethylbenzene, 16.24 ml) then dropwise piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (4.4 g, 4.2 ml) in THF (50 ml). The mixture was stirred between −5° C. to 0° C. for 3 hour and 1-bromo-3-methoxypropane (4.97 g) was added slowly at 0° C. The mixture was then stirred overnight at RT, the solvent was evaporated off, the residue taken up in ethyl acetate and washed with water then brine. The layers were separated, the organic layer dried over sodium sulphate and then evaporated off to give the desired 4-(3-methoxy-propyl)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester a light brown oil (6.058 g) oil that was used in next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258158B2
Source datasetuspto-grants-2012_09
ORD IDord-149180be133d4c7bbe90ae164938b1a4
Source noteuspto-grants-2012_09