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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109165Generated: October 25, 2026

Trifluoroacetic acid → rac-cis-1,3,3a,4,5,9b-hexahydro-6-methoxy-2H-benzo[e]indol-2-one

https://huagongshe.com/reaction/1109165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantSodium HydroxideHCID 14798—
Reactant1,3,4,5-tetrahydro-6-methoxy-2H-benzo[e]indol-2-oneHCID 19021475—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productrac-cis-1,3,3a,4,5,9b-hexahydro-6-methoxy-2H-benzo[e]indol-2-oneHCID 13171842381%

Reaction Steps

A suspension of 150 g (0.7 mol) of 1,3,4,5-tetrahydro-6-methoxy-2H-benzo[e]indol-2-one in 1.5 l of methylene chloride was treated with 333 ml (2.1 mol) of triethylsilane and then slowly dropwise at 0° and while stirring with 240 ml of trifluoroacetic acid. After stirring for three hours 400 ml of 20% sodium hydroxide solution were added slowly while cooling until a pH of 14 had been reached. Subsequently, the mixture was poured into water and extracted with methylene chloride. The organic phase was washed with sodium chloride solution, dried with sodium sulphate, filtered and evaporated. The residue was treated with 500 ml of ether, whereupon the solid was filtered off and dried at 50°/20 Torr. There were obtained 123 g (81%) of rac-cis-1,3,3a, 4,5,9b-hexahydro-6-methoxy-2H-benzo[e]indol-2-one with m.p. 192°-194°. The material showed a Rf value of 0.14 in a thin-layer chromatogram (silica gel, ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05318966
Source datasetuspto-grants-1994_06
ORD IDord-1e002856fc434872acccc7c80d103156
Source noteuspto-grants-1994_06