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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647482Generated: October 30, 2026

2-Bromoethanol → HCID 11740620, compound

https://huagongshe.com/reaction/1647482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantHCID 10020017HCID 10020017—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11740620HCID 11740620—

Reaction Steps

To a solution of 3-isobutyryl-4-(4-fluoro-2-methyl-phenylamino)-8-hydroxyquinoline (5 g, 14.8 mmol) in dry tetrahydrofuran (250 ml) was added potassium t-butoxide (2.49 g, 22.2 mmol), followed by 2-bromoethanol (3.69 g, 29.6 mmol). The stirred mixture was heated under reflux for 16 hours, then a further quantity of potassium t-butoxide (2.49 g, 22.2 mmol) and 2-bromoethanol (3.69 g, 29.6 mmol) added, and heating continued for 2 days. The solvent was evaporated, and the residue treated with aqueous sodium bicarbonate and extracted into dichloromethane. The extracts were dried and evaporated to an oil, which was purified by flash chromatography (silica gel, dichloromethane/methanol) and recrystallisation from ether to yield 3-isobutyryl-4-(4-fluoro-2-methylphenylamino-8-(2-hydroxyethoxy) (1.97 g), m.p. 183°-185°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432182
Source datasetuspto-grants-1995_07
ORD IDord-921ec522be5a4871b2587249dfde6672
Source noteuspto-grants-1995_07