HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1528168Erstellt: 26. Oktober 2026
Methanol → 7-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-one
https://huagongshe.com/reaction/1528168
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methanol | HCID 887 | — |
| Edukt | Boron tribromide | HCID 25134 | — |
| Edukt | 7-Methoxy-2-methylisoindolin-1-one | HCID 84717848 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 7-hydroxy-2-methyl-2,3-dihydro-1H-isoindol-1-one | HCID 58522544 | 76,3% |
Reaktionsschritte
100 ml of a 1 M solution of boron tribromide in dichloromethane at −78° C. were added dropwise to a solution of 3.7 g of 7-methoxy-2-methyl-2,3-dihydroisoindol-1-one in 50 ml of dichloromethane. The reaction medium was stirred at −78° C. for 1 hour and then left to return to 0° C. for 1 hour. The reaction medium was cooled to −78° C. and then slowly hydrolyzed by adding, dropwise, 20 ml of methanol (temperature below −60° C.). The reaction medium was washed with 30 ml of a 1 M sodium dihydrogen phosphate solution and the aqueous phase was extracted with ethyl acetate (2×50 ml). The organic phases were combined, dried over magnesium sulfate and evaporated. The residue was triturated with diethyl ether. 2.6 g of 7-hydroxy-2-methyl-2,3-dihydroisoindol-1-one were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09090596B2 |
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| Quelldatensatz | uspto-grants-2015_07 |
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| ORD ID | ord-e4f7189123084555ae7895ab2a99ae59 |
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| Quellennotiz | uspto-grants-2015_07 |
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