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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263418Generated: October 30, 2026

Hydrochloric Acid → HCID 18654742, compound

https://huagongshe.com/reaction/263418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(+)(2aR,4S)-1-benzoyl-6-bromo-4-(di-n-propylamino)1,2,2a,3,4,5-hexahydrobenz[cd]indoleHCID 10813042—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 18654742HCID 1865474298.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 12.8 g (29 mmol) of (+)(2aR,4S)-1-benzoyl-6-bromo-4-(di-n-propylamino) -1,2,2a,3,4,5-hexahydrobenz[cd]indole in 200 ml of tetrahydrofuran cooled to -78° C. under a nitrogen atmosphere was added 20 ml (32 mmol) of a 1.6M solution of n-butyllithium in hexane. The reaction mixture was stirred at -78° C. for 30 minutes and then allowed to warm to -20° C. To the reaction mixture was added 50 ml of a 1N hydrochloric acid solution. The mixture was 5 extracted once with diethyl ether. The acidic solution was made alkaline with the addition of cold 5N sodium hydroxide solution. The basic mixture was extracted twice with methylene chloride. The combined organic solution was washed with a saturated sodium chloride solution. The methylene chloride solution was dried over magnesium sulfate and evaporated to give 9.6 g of (-)(2aR,4S)-6-bromo-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643910
Source datasetuspto-grants-1997_07
ORD IDord-6d8ee212ad654ff9bf008b8532ce8902
Source noteuspto-grants-1997_07