HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Methyl 2-amino-1,3-benzoxazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Methyl 3-amino-2-hydroxybenzoate | HCID 12782444 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-amino-1,3-benzoxazole-7-carboxylate | HCID 66940222 | 76% |
Reaction Steps
A mixture of 913 mg (5.46 mmol) 3-amino-2-hydroxy-benzoic acid methyl ester, 894 mg (8.19 mmol) of cyanogen bromide, 14.4 mL of ethanol and 1.6 mL of water was heated under reflux for 1 h. Ethanol was evaporated under reduced pressure and 20 mL of 2 N aq. Na2CO3 was added to the residue. The precipitated solid was filtered and washed with water. The remaining product was treated with methanol and the soluble filtrate containing the product was evaporated in vacuo to provide 797 mg (4.15 mmol, 76%) of 2-amino-benzooxazole-7-carboxylic acid methyl ester. LCMS: 193 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598353B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-c2c03cb86bb64ecdbf1fe2004e317c7a |
| Source note | uspto-grants-2013_12 |