HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22012989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22013049 | HCID 22013049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22012989 | HCID 22012989 | — |
Reaction Steps
To a suspension of 0.05 g of sodium hydride (60%) in 5 ml of N,N-dimethylformamide was added dropwise a solution of 0.36 g of 3,3-bis((1,1-dimethylethoxy)carbonylmethyl)indolin-2-one in 5 ml of N,N-dimethylformamide at 0° C. in a nitrogen stream. After stirring the mixture at that temperature for 30 minutes, 0.12 ml of benzyl bromide was added thereto. The whole mixture was stirred for 1 hour and then concentrated. Chloroform was added to the concentrate, and the mixture was washed with an aqueous solution of sodium chloride. The organic layer was dried over anhydrous sodium sulfate and concentrated to obtain 1-benzyl-3,3-bis((1,1-dimethylethoxy)carbonylmethyl)indolin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06031111 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-71e35d1ba6b14c60932cb71726a21b36 |
| Source note | uspto-grants-2000_02 |