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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026633Generated: October 25, 2026

Methanol → cis-6-cyclopropyl-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole hydrochloride

https://huagongshe.com/reaction/1026633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactantcis-2-benzyl-6-cyclopropyl-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindoleHCID 70664536—
SolventTolueneHCID 1140—
Productcis-6-cyclopropyl-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole hydrochlorideHCID 706644879.3%

Reaction Conditions

Temperature160 °C

Reaction Steps

cis-2-Benzyl-6-cyclopropyl-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole (0.359 mmol, 75 mg) was dissolved in toluene (1 ml). ACE-Cl (1.654 mmol, 182 μl) was added and the reaction mixture; was heated in a microwave reactor at 160° C. for 15 minutes. MeOH (1 ml) was added and the mixture was again heated in a microwave reactor at 160° C. for 5 minutes. The resulting mixture was passed through an SCX cartridge and the resulting filtrate was concentrated in vacuo to give a crude residue that was purified by preparative-HPLC. To the pure fractions was added HCl in ether (1 ml) and the resulting solution was concentrated in vacuo to afford cis-6-cyclopropyl-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole hydrochloride (8.8 mg), m/z: 228.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729274B2
Source datasetuspto-grants-2014_05
ORD IDord-4813c960fcf740f886eab183ed5ab2ca
Source noteuspto-grants-2014_05