HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12878956, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | HCID 23463634 | HCID 23463634 | — |
| Catalyst | Pyridinium chloride | HCID 10176127 | — |
| Product | HCID 12878956 | HCID 12878956 | — |
Reaction Steps
A mixture of 32 g of o-aminothiophenol, 70.7 g of p-chlorobenzalmalonate and 1.4 g of pyridine hydrochloride was heated at about 180° C. until no further ethanol was distilled out (for about 4 hours). After allowing the reaction mixture to cool, a mixture of benzene-petroleum ether was added to the reaction mixture which was then thoroughly stirred and filtered. The resulting filter cake was recrystallized from chloroform-petroleum ether to obtain 54.5 g of 2-(p-chlorophenyl)-2,3-dihydro-3-ethoxycarbonyl-1,5-benzothiazepin-4(5H)-one as colorless needles having a melting point of 206° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04264497 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-76aa82021c8d4430905b1e656bb666a1 |
| Source note | uspto-grants-1981_04 |