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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109211Generated: October 30, 2026

Ammonium Chloride → rac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-propyl-1H-benzo[e]indole

https://huagongshe.com/reaction/1109211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantrac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-propionyl-1H-benzo[e]indoleHCID 131718473—
SolventTetrahydrofuranHCID 8028—
Productrac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-propyl-1H-benzo[e]indoleHCID 7069468793.1%

Reaction Steps

0.90 g (0.0232 mol) of lithium aluminum hydride was suspended in 40 ml of THF under argon. A solution of 3.0 g (0.0116 mol) of rac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-propionyl-1H-benzo[e]indole in 50 ml of THF was added dropwise thereto and the mixture was boiled under reflux for 1 hour. 25 ml of a saturated aqueous NH4Cl solution was cautiously added dropwise thereto, the mixture was filtered and the filtrate was extracted with ethyl acetate. The organic phase was washed with water, dried with MgSO4, filtered and concentrated. By chromatography of the residue over silica gel with CH2Cl2 /MeOH 49:1 there were obtained 2.65 g (93%) of rac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-propyl-1H-benzo[e]indole as a colorless, oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05318967
Source datasetuspto-grants-1994_06
ORD IDord-c83643d80ce145528222a2aaddc033dd
Source noteuspto-grants-1994_06