HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 2,4-bis(benzyloxy)-6-bromo-5-hydroxynicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 71281752 | HCID 71281752 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 2,4-bis(benzyloxy)-6-bromo-5-hydroxynicotinate | HCID 89421752 | 68% |
Reaction Steps
A mixture of benzyl 2,4-bis(benzyloxy)-5-hydroxynicotinate (0.29 g, 0.66 mmol) and NBS (0.13 g, 0.72 mmol) in DMF (1.2 mL) was stirred at room temperature for 5 min then treated with water. The mixture was extracted with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, evaporated and purified by silica chromatography (0-30% ethyl acetate in hexanes) to give benzyl 2,4-bis(benzyloxy)-6-bromo-5-hydroxynicotinate (0.23 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409905B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-21ba3dc850684b919a1ed23e40cc7feb |
| Source note | uspto-grants-2016_08 |