HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649376Generated: October 29, 2026
Acetic Acid Mixture with Hydrobromic Acid → HCID 22837852, compound
https://huagongshe.com/reaction/649376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Reactant | HCID 54033484 | HCID 54033484 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22837852 | HCID 22837852 | — |
Reaction Steps
In 5 ml of acetic acid is dissolved 1.4 g of tert-butyl 3(R)-benzyloxycarbonylamino-4-oxo-7-trifluoromethyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate, and 10 ml of 30% hydrogen bromide-acetic acid solution is added to the solution, followed by allowing the mixture to stand at room temperature for 4 hours. Petroleum ether (100 ml) is added to the reaction solution, and the mixture is thoroughly shaken, followed by decanting the supernatant. After petroleum ether is again added to repeat the same procedure, the residue is dissolved in a mixture of ethyl acetate and benzene, and the mixture is concentrated to dryness under reduced pressure. Petroleum ether is added to the residue to give 0.75 g of 3(R)-amino-4-oxo-7-trifluoromethyl-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetic acid.hydrobromide as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04739066 |
|---|
| Source dataset | uspto-grants-1988_04 |
|---|
| ORD ID | ord-d94f1a59a4e749d591f970392e5caced |
|---|
| Source note | uspto-grants-1988_04 |
|---|