HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-(3-bromo-5-chloro-benzyl)-7-methoxy-4H-benzo[1,4]oxazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Methoxy-2H-1,4-benzoxazin-3(4H)-one | HCID 11600770 | — |
| Reactant | 1-Bromo-3-(bromomethyl)-5-chlorobenzene | HCID 22324264 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-bromo-5-chloro-benzyl)-7-methoxy-4H-benzo[1,4]oxazin-3-one | HCID 22324262 | 84% |
Reaction Steps
0.5 grams of 7-methoxy-1,4-benzoxazin-3-one (2.8 mmole) was dissolved in 10 ml of dimethylformamide and cooled in an ice bath. 0.17 grams (3.5 mmole) of sodium hydride (60% wt. inn oil) was added, and after 5 minutes 0.8 grams (2.9 mmole) of 3-bromo-5-chloro-benzylbromide was added all at once. The mixture was stirred at ice bath temperature for 1 hour, and then quenched by addition of 1% hydrochloric acid. The product was extracted with ethyl acetate, that was evaporated under reduced pressure to give an oil which was chromatographed via medium pressure eluting with 10% ethyl acetate in hexanes to yield 0.9 grams of 4-(3-bromo-5-chloro-benzyl)-7-methoxy-4H-benzo[1,4]oxazin-3-one as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943169B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-8186f3ff87794e9c94cb18cc47c30c07 |
| Source note | uspto-grants-2005_09 |