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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580315Generated: October 26, 2026

Water → 1,4-Methanonaphthalen-2(1H)-one, 3,4-dihydro-

https://huagongshe.com/reaction/1580315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodiumHCID 5360545—
ReactantN-(3,4-Dihydro-1,4-methanonaphthalen-2(1H)-ylidene)hydroxylamineHCID 71356783—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product1,4-Methanonaphthalen-2(1H)-one, 3,4-dihydro-HCID 575764—

Reaction Steps

A solution of benzonorbornen-2-one oxime (2g.) in absolute ethanol (120ml.) was heated to reflux under nitrogen and sodium metal (12 g.) was added in small portions with continuous stirring. The reaction mixture was then refluxed for 30 minutes. This viscous suspension was then cooled to room temperature, 100 ml. of water added and the reaction mixture agitated until a clear solution was obtained. This was extracted with ether and the ether extract worked up to give an oil which was dissolved in chloroform and extracted with 10% HCl solution. Removal of water and excess HCl under vacuum from this extract gave a white solid (1g., 40%). The white solid was analyzed by infra-red, nuclear magnetic resonance and elemental analysis techniques and was determined to be the 1,2,3,4-tetrahydro-1,4-methanonaphthalen-endo-2-amine hydrochloride, C11H14NCl (m.p. 230°-231°C). Basification of a sample of this material with 10% NaOH gave, on ether extraction, the required amine as a pale yellow oil which was also analyzed by infra-red, and nuclear magnetic resonance techniques, and the empirical formula was determined to be C11H13N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932512
Source datasetuspto-grants-1976_01
ORD IDord-d65f1e309a404ed7b1c0b904e0fa3bf3
Source noteuspto-grants-1976_01