HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl ester | HCID 22986101 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester | HCID 22986100 | 83.3% |
Reaction Steps
A mixture of (8(a)) (0.60 g), allyl bromide (0.28 g), potassium carbonate (0.59 g) and DMF (20 ml) was stirred for 3 hours at ambient temperature under an argon atmosphere. The dimethyl formamide was then evaporated under reduced pressure and the residue dissolved in ethyl acetate (50 ml) and water (50 ml). The organic phase was separated, washed with brine (50 ml), dried over magnesium sulphate and evaporated under reduced pressure to dryness to give 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester (8(b)) as a yellow oil (0.571 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232338B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-793cee6126f848ceb335d8fb4c0a33b6 |
| Source note | uspto-grants-2001_05 |