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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733214Generated: October 26, 2026

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

https://huagongshe.com/reaction/733214

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-2-propyl-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 numberUS07589117B2
Source datasetuspto-grants-2009_09
ORD IDord-d2087421d4314cd886e68a6d22f2b0c1
Source noteuspto-grants-2009_09