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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049998Generated: October 26, 2026

Formaldehyde → HCID 13179542, compound

https://huagongshe.com/reaction/2049998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20343178HCID 20343178—
Reactant6-(Morpholin-4-yl)-3,4-dihydronaphthalen-1(2H)-one--hydrogen chloride (1/1)HCID 20343179—
Reactant1-Benzhydrylpiperazinium chlorideHCID 44146891—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 13179542HCID 13179542—

Reaction Steps

In 50 ml. of ethanol was dissolved a mixture of 2 g. of 6-morpholino-3,4-dihydro-1(2H)-naphthalenone hydrochloride, 4 g. of 1-benzhydrylpiperazine hydrochloride and 4 g. of a 37% aqueous solution of formalin. The solution was allowed to stand at room temperature for 10 days, after which it was neutralized with an aqueous solution of sodium hydrogen carbonate and extracted with 100 ml. of chloroform. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. By the above procedure there was obtained 5 g. of 2-[(4-benzhydryl-1-piperazinyl)methyl]-6-morpholino-3,4-dihydro-1(2H)-naphthalenone as colorless oil. IRνc=o neat 1665 cm-1. This oil was dissolved in 50 ml. of methanol and stirred with 3 g. of sodium borohydride at room temperature for 30 minutes. The reaction mixture was diluted with 500 ml. of water and extracted with 150 ml. of chloroform. The extract was dried and distilled under reduced pressure to remove the solvent, whereupon 4.5 g. of 2-[(4-benzhydryl-1-piperazinyl)methyl]-6-morpholino-1,2,3,4-tetrahydro-1-naphthalenol was obtained as an oil. A portion of this oil was purified by chromatography on a column of silica gel and lead to its fumarate melting at 184°-187° C.(decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04199582
Source datasetuspto-grants-1980_04
ORD IDord-26d58f603c2c4b0eb37625ee4be2dee9
Source noteuspto-grants-1980_04