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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580050Generated: October 30, 2026

Acetic Acid → HCID 13477125, compound

https://huagongshe.com/reaction/580050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13477123HCID 13477123—
SolventFormaldehydeHCID 712—
SolventAcetonitrileHCID 6342—
ProductHCID 13477125HCID 13477125—

Reaction Steps

To a solution of 2.8 g (0.011 m) of 2-(6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethylamine of Example 6 in 60 ml of acetonitrile and 2.7 ml of 37% aqueous formaldehyde (0.1 m), 2.05 g (0.033 m) of NaBH3CN was added. There was a slightly exothermic reaction. Glacial acetic acid (2 ml) was added over 10 minutes and the reaction was stirred at ambient temperature for 2 hours. An additional 2 ml of glacial acetic acid was added and stirring was continued for 30 minutes. The solvent was evaporated under reduced pressure and the residue was treated with 60 ml of 2N KOH. The resulting mixture was extracted three times with ether. The combined ether extracts were washed with 60 ml of 0.5N KOH and then extracted three times with 1N HCl. The aqueous acidic extracts were combined and neutralized with solid KOH and then extracted with ether. The dried (Na2SO4 ) organic phase was filtered and ethereal HCl was added to precipitate 2-(6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl)-N,N-dimethylethylamine hydrochloride, 1.4 g (40%), m.p. 175°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751238
Source datasetuspto-grants-1988_06
ORD IDord-41486ea29e744f58b46be8b3fc5d8c0a
Source noteuspto-grants-1988_06