Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730346Generated: November 1, 2026

Ethanol → HCID 21413266, compound

https://huagongshe.com/reaction/1730346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 21413254HCID 21413254—
SolventHydrochloric AcidHCID 313—
ProductHCID 21413266HCID 2141326642.4%

Reaction Steps

A solution of 1-[2-(o-nitrophenyl)ethyl]-4-benzamidopiperidine (4.25 g.) inabsolute ethanol (150 ml.) was added over 50 minutes to stirred stannous chloride (10.82 g.) in concentrated hydrochloric acid (12 ml.). and water (7.5 ml.) at 60°-70° C. After addition, the mixture was stirred at this temperature for 4 hours before cooling and evaporating theethanol. Continuous extraction into chloroform of the neutralised (with 2N sodium hydroxide solution) aqueous fraction gave the title compound (1.65 g.). The aqueous layer after extraction was made alkaline with 2N sodium hydroxide solution and extracted with more chloroform to give a further batch of the title compound (2.36 g.). The total product was crystallised from ethanolic hydrogen chloride and ether to give the hydrochloride of the title compound (2.75 g.), m.p. 263.8° C. (Found: C, 60.3; H, 7.0; N, 10.5. C20H25N3O. 2HCl requires C, 60.6; H, 6.9; N, 10.60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992389
Source datasetuspto-grants-1976_11
ORD IDord-07b81cf82d464a2e8a2612ee03d87669
Source noteuspto-grants-1976_11