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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750638Generated: October 27, 2026

N-Methylphthalimide → 3-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-one

https://huagongshe.com/reaction/750638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylphthalimideHCID 11074—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-oneHCID 275258832.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaBH4 (566 mg, 14.91 mmol) was added to a stirring solution of 2-methyl-isoindole-1,3-dione (2.0 g, 12.42 mmol) in methanol (20 mL) at 0° C. Stirring at 0° C. was maintained for 1 hour, then the reaction was warmed to room temperature. Additional NaBH4 (566 mg, 14.91 mmol) was added in order to push the reaction to completion. The reaction was then quenched with acetic acid (5 mL) and partitioned between water and dichloromethane. The organic layer was washed several times with water and concentrated under vacuum to give 659 mg of the sub-title compound as a white solid. MS: ESI (positive): 164 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405215B2
Source datasetuspto-grants-2008_07
ORD IDord-360f565a6cb1457ab11a4310c4e227cc
Source noteuspto-grants-2008_07