Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433987Generated: October 29, 2026

Propargyl bromide → HCID 20610736, compound

https://huagongshe.com/reaction/433987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69666208HCID 69666208—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 20610736HCID 2061073694.9%

Reaction Steps

(2R)-2-(1H-Imidazo[4,5-c]quinolin-1-yl)butan-1-ol (19 g, 78.8 mmol) was added to a mixture of sodium hydroxide (124 mL of 50%), dichloromethane (150 mL), benzyltrimethyl ammonium chloride (0.73 g), and propargyl bromide (11.4 mL, 102 mmol). The reaction mixture was allowed to stir at ambient temperature overnight. The reaction mixture was diluted with dichloromethane and water. The aqueous fraction was extracted multiple times with dichloromethane. The organic fractions were combined, washed with water, dried over magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate to provide 20.9 g of 1-{(1R)-1-[(prop-2-ynyloxy)methyl]propyl}-1H-imidazo[4,5-c]quinoline as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670372B2
Source datasetuspto-grants-2003_12
ORD IDord-0116d1286be14fb996c12e3adaf35a9a
Source noteuspto-grants-2003_12