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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026627Generated: October 26, 2026

N-benzyl-3-chloro-N-(2-methylallyl)-1,2-dihydrocyclobutabenzene-1-carboxamide → trans-2-benzyl-6-chloro-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindol-1-one

https://huagongshe.com/reaction/1026627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyl-3-chloro-N-(2-methylallyl)-1,2-dihydrocyclobutabenzene-1-carboxamideHCID 70664766—
SolventBromobenzeneHCID 7961—
Producttrans-2-benzyl-6-chloro-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindol-1-oneHCID 7066518412.3%

Reaction Steps

A solution of N-benzyl-3-chloro-N-(2-methylallyl)-1,2-dihydrocyclobutabenzene-1-carboxamide (5.52 mmol, 1.8 g) in bromobenzene (21 ml) was irradiated in a microwave for 30 min at 210 degrees. The bromobenzene was removed under reduced pressure and then purified by flash chromatographed using ethyl acetate in heptane (10 to 20%) to afford trans-2-benzyl-6-chloro-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindol-1-one (221 mg, 12% yield), followed by cis-2-benzyl-6-chloro-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindol-1-one (649 mg, 36% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729274B2
Source datasetuspto-grants-2014_05
ORD IDord-45f78ba227804ec7bf177ba8d35e2084
Source noteuspto-grants-2014_05