HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → 2-(Chloromethyl)-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Ethyl 2-chloroethanecarboximidate hydrochloride | HCID 12470659 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Chloromethyl)-1,3-benzoxazole | HCID 2061989 | 65% |
Reaction Steps
A mixture of o-aminophenol (4.00 g, 36.6 mmol) and ethyl chloroacetimidate hydrochloride (8.68 g, 54.98 mmol) in ethanol (55 mL) was heated at reflux for 18 hours. The reaction mixture was cooled to room temperature and vacuum filtered. The filtrate was concentrated in vacuo, diluted with methylene chloride and filtered again. The methylene chloride filtrate was dried (MgSO4) and concentrated to afford 3.99 g (65%) of product as a brown oil which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05104892 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-3e0fa8619f6d43a290051e3fc539557d |
| Source note | uspto-grants-1992_04 |