HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(2-Methylthiazol-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylthiazol-5-amine hydrochloride | HCID 86715558 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Methylthiazol-5-yl)acetamide | HCID 73554716 | 77.6% |
Reaction Steps
To a solution of Et3N (1.4 ml, 10 mmol) and 2-methylthiazol-5-amine hydrochloride (1 g, 6.6 mmol) in DCM (30 mL) was added Ac2O (0.94 mL, 10 mmol). The mixture was stirred at room temperature for 3 h. The reaction solution was concentrated, deposited onto silica gel and loaded onto a silica gel column and eluted with EA to give the title compound (0.8 g, yield: 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388180B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-9260f1e1a35e46948e3fb32945d1b786 |
| Source note | uspto-grants-2016_07 |