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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579816Generated: November 3, 2026

6,7,8,9,10,11-Hexahydro-3-Methoxy-5-Methyl-5,10-Methano-5H-Benzocyclononen-12-Amine → 5-Ethyl-6,7,8,9,10,11-Hexahydro-3-Methoxy-5,10-Methano-5H-Benzocyclononen-12-Imine

https://huagongshe.com/reaction/1579816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6,7,8,9,10,11-Hexahydro-3-Methoxy-5-Methyl-5,10-Methano-5H-Benzocyclononen-12-AmineHCID 21410070—
Reactant5-Ethyl-6,7,8,9,10,11-Hexahydro-3-Methoxy-5,10-Methano-5H-Benzocyclononen-12-OneHCID 21410072—
Product5-Ethyl-6,7,8,9,10,11-Hexahydro-3-Methoxy-5,10-Methano-5H-Benzocyclononen-12-ImineHCID 21410136—

Reaction Steps

Using a procedure analogous to that described in Example XXVIIA for the preparation of 6,7,8,9,10,11-hexahydro-3-methoxy-5-methyl-5,10-methano-5H-benzocyclononen-12-amine there is obtained from 3.5 g. of 5-ethyl-6,7,8,9,10,11-hexahydro-3-methoxy-5,10-methano-5H-benzocyclononen-12-one, oxime 1.6 g. of the title product, b.p. 150°-160° C. (0.5 mm.). I.R. Analysis: 6.1 μ. Addition of ethereal hydrogen chloride to the title product in ether gives the hydrochloride salt, m.p. 252°-255° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931328
Source datasetuspto-grants-1976_01
ORD IDord-f66195921bf64033ab94a9a55f6cd86d
Source noteuspto-grants-1976_01