HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 6-Methoxy-3-(piperidin-4-yl)-1,2-benzoxazole--hydrogen bromide (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Benzyl 4-(6-methoxy-1,2-benzoxazol-3-yl)piperidine-1-carboxylate | HCID 13076417 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Methoxy-3-(piperidin-4-yl)-1,2-benzoxazole--hydrogen bromide (1/1) | HCID 13076429 | 79.8% |
Reaction Steps
To 30 ml of a saturated solution of hydrogen bromide and acetic acid was added, with stirring, 0.88 g of 4-(6-methoxy-1,2-benzisoxazol-3-yl)-1-piperidine carboxylic acid phenylmethyl ester. The reaction was stirred at ambient temperature for 55 min. The resultant solid was collected, washed with ether and dried to yield 0.5 g (79.8%) of product. Recrystallization from methanol gave the analytical sample, mp 258°-260°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355037 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-45019cc267944e61855e1ad52756722d |
| Source note | uspto-grants-1982_10 |