Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109196Generated: October 30, 2026

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

https://huagongshe.com/reaction/1109196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantCyclopentylacetyl chlorideHCID 3485182—
Reactantrac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indoleHCID 101650127—
SolventDichloromethaneHCID 6344—
Productrac-cis-3-(cyclopentylacetyl)-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indoleHCID 13171845884.3%

Reaction Steps

5.0 g (0.0246 mol) of rac-cis-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indole were dissolved in 100 ml of CH2Cl2, 4.1 ml (0.0295 mol) of triethylamine were added thereto and a solution of 4.3 ml (0.0295 mol) of 3-cyclopentylacetyl chloride in 40 ml of CH2Cl2 was added dropwise thereto at 15° under argon. The mixture was stirred at room temperature for 1/2 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 3:1 there were obtained 6.50 g (84%) of pale yellow oily rac-cis-3-(cyclopentylacetyl)-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benzo[e]indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05318967
Source datasetuspto-grants-1994_06
ORD IDord-bdf9b97d3e4f40ee817924bcd4443fc7
Source noteuspto-grants-1994_06