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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850812Generated: November 1, 2026

Phosphorus oxychloride → Ethyl 6-bromo-4-chloroquinoline-3-carboxylate

https://huagongshe.com/reaction/1850812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiethyl 2-((4-bromophenylamino)methylene)malonateHCID 1591151—
ProductEthyl 6-bromo-4-chloroquinoline-3-carboxylateHCID 276413852.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

A 20 mL microwave vial was charged with 2-[(4-bromo-phenylamino)methylene]malonic acid diethyl ester (1.711 g, 5.0 mmol) and POCl3 (phosphoryl chloride, 10.0 mL, 16.8 g, 109 mmol). The vial was capped and the mixture was microwave heated stepwise up to 180° C. (watching the pressure) over 5 min and then kept at 180° C. for 30 min. Excess POCl3 was evaporated and the residue partitioned between CH2Cl2 (40 mL) and 2 N NaOH (aq) (40 mL). The aqueous layer was extracted with CH2Cl2 (2×40 mL). The organic layers were combined, dried with Na2CO3 and evaporated. The residue was purified on column (silica gel, CH2Cl2 as eluent). Pure fractions were pooled, evaporated and the residue dried under vacuum to give 0.821 g (52%) of 6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester. MS (ESI+) m/z 314, 316 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957092B2
Source datasetuspto-grants-2015_02
ORD IDord-33bc0e6da21641eebdd59782a6a2ebaa
Source noteuspto-grants-2015_02