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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684413Generated: October 30, 2026

Boron tribromide → Diethyl (6-hydroxy-3-quinolyl)methylacetamidomalonate

https://huagongshe.com/reaction/1684413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantDiethyl (6-methoxy-3-quinolyl)methylacetamidomalonateHCID 57184951—
SolventDichloromethaneHCID 6344—
ProductDiethyl (6-hydroxy-3-quinolyl)methylacetamidomalonateHCID 5723450111.5%

Reaction Steps

To a solution of 0.39 g (1 mmol) of diethyl (6-methoxy-3-quinolyl)methylacetamidomalonate in 10 mL of dry methylene chloride was added dropwise at -70° C. a 1M solution of boron tribromide in methylene chloride. The reaction temperature was gradually raised to room temperature while stirring overnight. Then, the reaction mixture was poured into ice water and extracted with methylene chloride. The organic layer was washed with water, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel, using 1:1 ethyl acetate/methylene chloride and then ethyl acetate as eluents, to give 43 mg (11.5%) of the desired product as a solid. TLC Rf =0.46 (ethyl acetate); NMR (CDCl3) δ 8.4 (1H, bs), 7.95 (1H, d), 7.7 (1H, bs), 7.35 (1H, dd), 7.1 (1H, d), 6.8 (1H, bs), 4.25 (4H, m), 3.8 (2H, bs), 2.0 (3H, s), 1.3 (6H, m); IR (KBr) ν 3700-2800, 1740, 1660, 1645, 1620, 1500 cm-1. The product has the structural formula: ##STR88##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639885
Source datasetuspto-grants-1997_06
ORD IDord-0615c483333d4d3f8de357519332168a
Source noteuspto-grants-1997_06