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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719859Generated: November 3, 2026

Formaldehyde → 9-Diethylaminomethyl-6-methyl-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoline-3,10-dione hydrochloride

https://huagongshe.com/reaction/1719859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDiethylammonium chlorideHCID 10197650—
Reactant6-Methyl-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoline-3,10-dioneHCID 13051767—
SolventAcetic AnhydrideHCID 7918—
Product9-Diethylaminomethyl-6-methyl-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoline-3,10-dione hydrochlorideHCID 20266053—

Reaction Steps

Diethylamine hydrochloride (8.3 g) is mixed with 6 ml of 37% formalin at room temperature for 30 minutes whereupon 40 ml of acetic anhydride is added dropwise at 60°-70° C. with stirring. After about 1 hour 11.5 g of 6-methyl-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoline-3,10-dione is added, and the resulting mixture is kept at 60°-70° C. for 3 hours. The reaction mixture is then concentrated under reduced pressure. To the residue is added 200 ml of acetone, and the mixture is heated under reflux for 10 minutes and then allowed to stand at room temperature. The precipitated crystals are collected by filtration and recrystallized from ethanol to give 7.0 g of 9-diethylaminomethyl-6-methyl-1,2,3,4,7,8,9,10-octahydro-benzo[f]quinoline-3,10-dione hydrochloride as colorless needles, melting at 196°-197° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543354
Source datasetuspto-grants-1985_09
ORD IDord-1832a03952ed41da9b9e82ffc0b26ac8
Source noteuspto-grants-1985_09