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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792905Generated: October 27, 2026

N-Propylphthalimide → 3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one

https://huagongshe.com/reaction/1792905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-PropylphthalimideHCID 79215—
SolventMethanolHCID 887—
SolventPotassium borohydrideHCID 4192641—
Product3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-oneHCID 401353466%

Reaction Conditions

Temperature20 °C

Reaction Steps

3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one is prepared as described in Example 1, starting with 1.5 g of N-propylphthalimide in 25 cm3 of methanol and 0.48 g of potassium borohydride. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours and is then cooled to a temperature in the region of 0° C. and distilled water is added dropwise. The methanol is then partially evaporated off under reduced pressure (2 kPa) at a temperature in the region of 35° C. and the residue is cooled to 0° C. The precipitate obtained is filtered off and then washed with cold water. The solid is taken up in dichloromethane and the solvent is then evaporated to dryness under reduced pressure (2 kPa) at a temperature in the region of 35° C. 1.0 g of 3-hydroxy-2propyl-2,3-dihydroisoindol-1-one is thus obtained in the form of a beige-colored powder. (Rf=0.6, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (30/70 by volume)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078428B2
Source datasetuspto-grants-2006_07
ORD IDord-b899b9d8d8054722b2f738da334d7782
Source noteuspto-grants-2006_07