HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Methyl 2,3-dihydro-2-(1-methylethyl)-1H-isoindole-1-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 2-(isoindolin-1-yl)acetate | HCID 58777828 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Methyl 2,3-dihydro-2-(1-methylethyl)-1H-isoindole-1-acetate | HCID 69219063 | — |
Reaction Steps
To the compound obtained from Step A (0.50 g, 2.61 mmol) in dichloroethane (46 mL) was added acetone (1.76 mL, 24.01 mmol) and sodium triacetoxyborohydride (2.48 g., 11.74 mmol). After 6 hours, the mixture was diluted with 1.0N NaOH (100 mL), and the organic portion was separated. The aqueous layer was extracted with DCM (3×100 mL). The combined DCM extracts were dried (MgSO4) and concentrated to dryness to afford about 0.60 g (99%). EIS-MS 235 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186715B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-e82a5906b4ff4eb5ae5943fa2e17d007 |
| Source note | uspto-grants-2007_03 |