HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1-Allyl-3,3-dimethoxyindolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,3-Dimethoxy-1,3-dihydro-2H-indol-2-one | HCID 15480745 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Allyl-3,3-dimethoxyindolin-2-one | HCID 22013110 | 90% |
Reaction Steps
A solution of 3.86 g of 3,3-dimethoxyindolin-2-one in 30 ml of N,N-dimethylformamide was added dropwise to a suspension of 1.2 g of sodium hydride (60%) in 40 ml of N,N-dimethylformamide at 0° C. in a nitrogen stream. After the mixture was stirred at that temperature for 30 minutes, 2.60 ml of allyl bromide was added thereto. The resulting mixture was stirred for 1 hour and then concentrated. Chloroform was added to the residue, and the mixture was washed with an aqueous solution of sodium chloride. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting crude product was purified by silica gel column chromatography (chloroform/hexane=1/1) to give 4.19 g (90%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06031111 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-8c887cde8339405880ad4feac1f4e4d0 |
| Source note | uspto-grants-2000_02 |