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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489266Generated: October 30, 2026

Hydrochloric Acid → HCID 22266526, compound

https://huagongshe.com/reaction/489266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22266478HCID 22266478—
SolventDichloromethaneHCID 6344—
ProductHCID 22266526HCID 2226652656.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

DMSO (0.54 mL, 7.64 mmol) was dissolved in methylene chloride (27 mL) and the solvent was cooled at −78° C. To the solvent were added dropwise oxalyl chloride (0.4 mL, 4.58 mL), a solution of 1-butyl-3-hydroxymethyl-5,6,7,8-tetrahydro-1H-quinoline-2-one (1-015-03) (0.9 g, 3.82 mmol) in methylene chloride (20 mL) and triethylamine (1.33 mL, 9.55 mmol), and then the reaction mixture was stirred at −78° C. for 5 min. The reaction mixture was gradually warmed to room temperature, and stirred at room temperature for 20 min. To the reaction mixture was added 1 mol/L diluted hydrochloric acid (50 mL), and the reaction mixture was extracted with ethyl acetate (200 mL), washed with aqueous saturated sodium hydrogen carbonate solution (50 mL) and brine (50 mL), dried over anhydrous magnesium sulfate, and evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (toluene/ethyl acetate) to give 1-butyl-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3-carboaldehyde (1-015-04) (0.5 g, 56%) as a pale yellow bubbly substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977266B2
Source datasetuspto-grants-2005_12
ORD IDord-799d3ab7cb9a48098de82077d09235e7
Source noteuspto-grants-2005_12