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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482886Generated: October 30, 2026

Formaldehyde → HCID 20244128, compound

https://huagongshe.com/reaction/482886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant95232-69-2HCID 20244129—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 20244128HCID 20244128—

Reaction Steps

Formaldehyde (37% w/w solution in water, 0.82 ml.), glacial acetic acid (0.82 ml.) and sodium cyanoborohydride (0.70 g.) were added to a solution of 2-[(1-aminocyclopropyl)methylthio]-3-phenylquinoline hydrochloride (1.2 g.) in ethanol (35 ml.). The mixture was stirred at ambient temperature for 4 hr., poured into saturated sodium bicarbonate solution (200 ml.), and extracted with ethyl acetate (3×100 ml.). The ethyl acetate extract was washed with brine (3×20 ml.), dried (Na2SO4), and evaporated in vacuo to dryness. The residual oil was chromatographed on silica gel (Merck Kieselgel 60, Art No. 9385, grain size 0.040-0.063 mm., 230-400 mesh ASTM; 180 g.) using chloroform as eluant. The relevant fraction was evaporated in vacuo to dryness, the residual oil (1.1 g.) was dissolved in methanol (20 ml.), and concentrated hydrochloric acid (0.3 ml.) was added. The resulting solution was evaporated in vacuo to dryness, and the residue was crystallised from a mixture of ethanol and diethyl ether, to yield 2-[(1-dimethylaminocyclopropyl)methylthio]-3-phenylquinoline hydrochloride, m.p. 219°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576953
Source datasetuspto-grants-1986_03
ORD IDord-8766f4d07c0741dfbc913e540eab0a33
Source noteuspto-grants-1986_03