HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Chloro-1,3-benzoxazol-6-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1,3-benzoxazol-6-OL | HCID 23441246 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-1,3-benzoxazol-6-yl acetate | HCID 18340179 | — |
Reaction Steps
Triethylamine (1.48 ml) was added to a suspension of 2-chloro-1,3-benzoxazol-6-ol (1.63 g) [see Preparation 34] in dichloromethane (20 ml), and after 5 minutes acetic anhydride (1.01 ml) was added. The reaction mixture was stirred at room temperature for 18 hours, after which time the solvent was removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0, changing to 40:10, changing to 0:100, by volume, hexane:ethyl acetate to afford 2-chloro-1,3-benzoxazol-6-yl acetate (1.63 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509464B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-6437e919629846eabefddf4632cf1e9e |
| Source note | uspto-grants-2003_01 |