HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 12609442, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2,3-dihydro-2-methyl-3-oxo-1H-isoindole-1-acetate | HCID 57321129 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12609442 | HCID 12609442 | 52.5% |
Reaction Steps
Sodium borohydride (4.1 g, 109.4 mmol) is added to a solution of 2,3-dihydro-2-methyl-3-oxo-1H-isoindole-1-acetic acid methyl ester (Synthesis, 1986:755) (4.8 g, 21.9 mmol) in 50 mL of MeOH at room temperature and stirred overnight. The reaction is quenched by addition of 100 mL of 2.0 N NaOH, and the MeOH is evaporated. The solution is extracted with CH2Cl2 (3×100 mL). The extracts are combined and dried over Na2SO4 and evaporated to give 2.2 g (52% yield) of 1,3-dihydro-2-methyl-3-(2-hydroxyethyl)-2H-isoindol-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06087364 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-78daec4284f94a84aed5463745c464e5 |
| Source note | uspto-grants-2000_07 |