HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 2-Methylbenzo[d]oxazol-6-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-1,3-benzoxazol-6-ol | HCID 676504 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methylbenzo[d]oxazol-6-yl acetate | HCID 15662263 | 88.1% |
Reaction Steps
A slurry of 2-methyl-1,3-benzoxazol-6-ol (7.1 g, 48.7 mmol) in THF (150 mL) was cooled to 10° C. and triethylamine (11.3 mL, 81.3 mmol) was added in one portion, followed by the addition of acetyl chloride (5.8 mL, 81.3 mmol) in small portions. After addition was completed the reaction mixture was stirred at room temperature over night, partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give sub-title compound (8.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524856B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-7985e78965b041ca9b3af9c38145e4bc |
| Source note | uspto-grants-2009_04 |