Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380103Generated: October 31, 2026

Ethanol → HCID 13606748, compound

https://huagongshe.com/reaction/1380103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
ReactantBoron tribromideHCID 25134—
ReactantHCID 13606747HCID 13606747—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 13606748HCID 13606748—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2.25 g (5.5 mm) of diethyl 1,4-dihydro-4-(2-methoxy-1-naphthalenyl)-2,6-dimethyl-3,5-pyridinedicarboxylate 20 in 12.0 mL of dry 1,2-dichloroethane was stirred under Ar at 25° C. and treated with 2.40 g (7.68 mm) of BBr3.CH3SCH3 complex. After stirring at 25° C. for 20 hours, 10.0 g of anhydrous powdered K2CO3 and 100 mL of absolute ethanol were added. Stirring was continued for 60 hours at 25°. The reaction was quenched with saturated aqueous NH4Cl and extracted with 500 ml of CH2Cl2. The organic layer was washed with pH 7 phosphate buffer and brine, dried (anhydrous Na2SO4), filtered, evaporated and flash chromatographed (silica gel, 2% acetone in CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579851
Source datasetuspto-grants-1986_04
ORD IDord-bd694a4f6ffc4d48af07a54c55e1e0f4
Source noteuspto-grants-1986_04