Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222002Generated: October 28, 2026

N-Carbethoxyphthalimide → 2-(2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-yl)isoindoline-1,3-dione

https://huagongshe.com/reaction/222002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-CarbethoxyphthalimideHCID 31187—
Reactant2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-amineHCID 58216602—
SolventChloroformHCID 6212—
Product2-(2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-yl)isoindoline-1,3-dioneHCID 58216606—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2-(4-bromophenyl)-5,8-dioxaspiro[3.4]octan-2-amine (7-1) (2.7 g, 9.50 mmol), ethyl 1,3-dioxo-1,3-dihydro-2H-isoindole-2-carboxylate (4.2 g, 19.0 mmol), and TEA (5.3 mL, 38.0 mmol) in CHCl3 (50 mL) was stirred at 70° C. for overnight. The solvent was evaporated under reduced pressure, and to the residue was added MeOH. The resulting solid was collected by filtration to give 2-[2-(4-bromophenyl)-5,8-dioxaspiro[3.4]oct-2-yl]-1H-isoindole-1,3(2H)-dione (7-2) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207169B2
Source datasetuspto-grants-2012_06
ORD IDord-a288a75db540489bb30c9030d98da4ef
Source noteuspto-grants-2012_06