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

HRID 1166472Notes

Reaction equation

[OH:1][N:2]1[C:6](=[O:7])[C:5]2=[CH:8][CH:9]=[CH:10][CH:11]=[C:4]2[C:3]1=[O:12].C1CCN2C(=NCCC2)CC1.[CH:24]1([CH2:30]Br)[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1>CN(C=O)C>[CH:24]1([CH2:30][O:1][N:2]2[C:3](=[O:12])[C:4]3[C:5](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]2=[O:7])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1

Participants

Conditions

Temperature: 55 °C

Procedure

N-hydroxylphthalimide (18.4 mmol, 3.0 g) was dissolved in anhydrous DMF (20 mL) under nitrogen. To the stirring solution, DBU (27.6 mmol, 4.13 mL) was injected followed by cyclohexylmethyl bromide (23.0 mmol, 3.21 mL) and the reaction was warmed to 55° C. After stirring for 15 hours, the reaction was cooled to room temperature and concentrated to a red oil. The reaction was partitioned between ethyl acetate and 1N HCl. The organic layer was washed with saturated aqueous sodium bicarbonate solution, brine and dried over magnesium sulfate. The solvent was removed under vacuum, and the crude product was triturated with hexanes providing 3.05 g (64%) of an off-white colored solid. H1-NMR (CDCl3): δ7.80 (2H,m), 7.73 (2H,m), 3.98 (2H,d), 2.03-1.65 20 (5H,m), 1.31-1.03 (6H,m).

Workup

temperaturethe reaction was cooled to room temperature
concentrationconcentrated to a red oil
customThe reaction was partitioned between ethyl acetate and 1N HCl
washThe organic layer was washed with saturated aqueous sodium bicarbonate solution, brine
dry with materialdried over magnesium sulfate
customThe solvent was removed under vacuum
customthe crude product was triturated with hexanes providing 3.05 g (64%) of an off-white colored solid

Sources & evidence

ORD record: ord-4d559cc6b10942a0b6ef98ad8cdf5e50
Source dataset: uspto-grants-2003_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06613743B2

Reaction notes

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