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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839135Generated: November 2, 2026

Dichloromethane → HCID 85883506, compound

https://huagongshe.com/reaction/1839135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22254448HCID 22254448—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 85883506HCID 85883506—

Reaction Steps

To 4-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)-1-butanol (1 g, 3.917 mmol), dichloromethane (14 mL), sodium hydroxide (14 mL of 50%), and benzyltrimethylammonium chloride (0.15 g, 0.783 mmol) were combined with stirring. Propargyl bromide (1.3 mL of 80% in toluene, 11.75 mmol) was added to the resulting mixture at ambient temperature. After the resulting reaction mixture was allowed to stir at ambient temperature for 1 hour, TLC analysis using 9/1 dichloromethane/methanol indicated incomplete reaction. After 18 hours HPLC monitoring indicated complete reaction. The two reaction layers were separated. The organic layer was washed with water (3×100 mL). All aqueous layers were combined and extracted with dichloromethane (3×100 mL). All organic layers were combined and washed with brine (3×100 mL). The brine layers were combined and extracted with dichloromethane (3×100 ML). All resulting organic layers were combined, dried with sodium sulfate, filtered, and concentrated under reduced pressure. HNMR analysis of the resulting dark oil was consistent with the desired product and some residual solvent. HPLC and LC/MS were consistent with the desired product (1.1 g) that was of sufficient purity for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677348B2
Source datasetuspto-grants-2004_01
ORD IDord-75524a9b45f349ec92dc08d0637227b4
Source noteuspto-grants-2004_01