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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970864Generated: October 30, 2026

Triethylamine → 2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/970864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
SolventDimethylformamideHCID 6228—
Product2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dioneHCID 1407441653%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of N-hydroxyphthalimide (10.0 g, 61.30 mmol) in DMF (40 mL) at RT was added NEt3 (9.40 mL, 67.43 mmol) and, in a dropwise fashion, (bromomethyl)cyclohexane (9.41 mL, 67.43 mmol). The reaction was then stirred for 15 hours at 50° C., after which it was allowed to cool to RT and then concentrated under vacuum. The residue was dissolved in Et2O (100 mL) and washed with water, brine, dried over MgSO4 and the solvent removed under reduced pressure. The residue was purified by column chromatography (eluting with CH2Cl2/PE, 1:1 to 3:1) to afford N-(cyclohexylmethoxy)phthalimide (8.40 g, 53%), as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312248B2
Source datasetuspto-grants-2007_12
ORD IDord-4f03575b0c2a4e62814cb4120aef2577
Source noteuspto-grants-2007_12