HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Rac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Z-6-chloro-3-(4-chloro-benzylidene)-1,3-dihydro-indol-2-one | HCID 962924 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Rac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-one | HCID 57507297 | 94.9% |
Reaction Steps
Sodium borohydride (3.0 g, 79 mmol) (Aldrich) was added in small portions to a suspension of 6-chloro-3-(4-chloro-benzylidene)-1,3-dihydro-indol-2-one (19 g, 66 mmol) (from example 76a supra) in methanol (200 mL) and DMSO (50 mL) at such a rate that gas evolution was not too vigorous. When the addition was complete, mixture was stirred at room temperature for 0.5 h-1 h. After water (200 mL) was added, the resulting precipitate was collected and dried to give 18.3 g of rac-6-chloro-3-(4-chloro-benzyl)-1,3-dihydro-indol-2-one as a light yellow solid. MS: 293 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058269B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-e584bd647ca54cc4981c54b738a5fb17 |
| Source note | uspto-grants-2011_11 |