HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 6-(tert-Butyl-dimethyl-silanyloxy)-1H-benzo[d][1,3]oxazine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 6-hydroxy-2,4-dihydro-1H-3,1-benzoxazine-2,4-dione | HCID 2759315 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(tert-Butyl-dimethyl-silanyloxy)-1H-benzo[d][1,3]oxazine-2,4-dione | HCID 11680883 | 96.6% |
Reaction Steps
To a mixture of 5-hydroxyisatoic anhydride (1.6 g, 9.0 mmol) and imidazole (670 mg, 9.9 mmol) in N,N-dimethylformamide (10 mL) was added tert-butyldimethylsilyl chloride (1.42 g, 9.45 mmol). After stirring for 2 h, the reaction mixture was diluted with ice and water. After warming to room temperature, the resulting precipitate was filtered and washed with water and hexane. The solid was vacuum dried at 55° C./0.1 mm for 14 h to give 2.55 g (96%) of the title compound as a light gray solid; mp 198-200° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313122B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-734904401dfc4cb2b5b0c6045c8b6158 |
| Source note | uspto-grants-2001_11 |