HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733206Generated: October 27, 2026
Water → 3-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-one
https://huagongshe.com/reaction/733206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | N-Methylphthalimide | HCID 11074 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-one | HCID 2752588 | 44.4% |
Reaction Steps
3.4 g of potassium borohydride are added slowly to a suspension of 10 g of N-methylphthalimide in 220 cm3 of methanol under an inert atmosphere. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours, followed by dropwise addition of 200 cm3 of distilled water. The solvent is then partially evaporated off (about 120 cm3) under reduced pressure (2 kPa) at a temperature in the region of 35° C., and the residue is diluted with 400 cm3 of distilled water. The mixture is extracted with 400 cm3 of ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 30° C. 4.5 g of 3-hydroxy-2-methyl-2,3-dihydroisoindol-1-one are thus obtained in the form of a white powder melting at 130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589117B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-c8ce6b1b5da54013bf86ee74e0ca34d7 |
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| Source note | uspto-grants-2009_09 |
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