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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109199Generated: October 31, 2026

Water → rac-cis-3-(3-cyclopentyl-propionyl)-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indole

https://huagongshe.com/reaction/1109199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-Cyclopentylpropionyl chlorideHCID 66039—
Reactantrac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indoleHCID 101650127—
SolventDichloromethaneHCID 6344—
Productrac-cis-3-(3-cyclopentyl-propionyl)-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indoleHCID 13171846272.5%

Reaction Steps

4.06 g (0.020 mol) of rac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indole were dissolved in 80 ml of CH2Cl2, 3.35 ml (0.024 mol) of triethylamine were added thereto and a solution of 3.7 ml (0.024 mol) of 3-cyclopentylpropionyl chloride in 40 ml of CH2Cl2 was added dropwise thereto at 20° under argon. The mixture was stirred at room temperature for 1 hour, then poured into water and extracted with CH2Cl2. The organic phase was washed with saturated aqueous NaHCO3 and NaCl solutions, dried with MgSO4, filtered and concentrated. By chromatography of the residue over silica gel with n-hexane/ethyl acetate 1:1 there were obtained 4.75 g (72.5%) of rac-cis-3-(3-cyclopentyl-propionyl)-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indole as a pale yellow, oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05318967
Source datasetuspto-grants-1994_06
ORD IDord-3f043f19ddc14706bce7aa3821783a8a
Source noteuspto-grants-1994_06