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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54507Generated: October 29, 2026

Iodoethane → (4aR)-(10bR)-8-chloro-4-ethyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one

https://huagongshe.com/reaction/54507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium HydroxideHCID 14798—
Reactant8-Chloro-1,4,4a,5,6,10b-hexahydro-2H-benzo[f]quinolin-3-oneHCID 10059992—
SolventTetrahydrofuranHCID 8028—
Product(4aR)-(10bR)-8-chloro-4-ethyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 54421716—

Reaction Steps

A 9.4 g portion of (4aR)-(10bR)-8-chloro-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one was combined in a flask with 94 ml of THF, 20 mL of 50% aqueous sodium hydroxide and 9.36 g of ethyl iodide, and was stirred at reflux, about 66°, for about 16 hours. The mixture was cooled to ambient temperature, and the layers were separated. The organic layer was evaporated to an oil, which was dissolved in ethyl acetate and extracted three times with 100 mL portions of water. It was then dried and evaporated to half its volume while heptane was added in portions. The resulting white crystalline product was filtered, washed with heptane and dried under vacuum at 25° to obtain 3.15 g of the desired product, m.p. 108°-110°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622962
Source datasetuspto-grants-1997_04
ORD IDord-00aee3684cec493a9e1704cc3d59637c
Source noteuspto-grants-1997_04