HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55341Generated: October 29, 2026
Hydrochloric Acid → HCID 18654742, compound
https://huagongshe.com/reaction/55341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (+)(2aR,4S)-1-benzoyl-6-bromo-4-(di-n-propylamino)1,2,2a,3,4,5-hexahydrobenz[cd]indole | HCID 10813042 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 18654742 | HCID 18654742 | 98.1% |
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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624944 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-dde82f3563d6473db64fab4a3dfd8575 |
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| Source note | uspto-grants-1997_04 |
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