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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653045Generated: October 26, 2026

3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline

https://huagongshe.com/reaction/653045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoquinolineHCID 21413—
ReactantN-(dimethoxyacetyl)morpholineHCID 21298597—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(Dimethoxyacetyl)quinolineHCID 14276934—

Reaction Steps

3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4O, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675186
Source datasetuspto-grants-1987_06
ORD IDord-08b32b1bda01412ca4af4d79f02e593d
Source noteuspto-grants-1987_06