HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → HCID 12878966, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | HCID 86737707 | HCID 86737707 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12878966 | HCID 12878966 | 27.4% |
Reaction Steps
A mixture of 32 g of o-aminothiophenol, 69.6 g of ethyl p-methoxybenzalmalonate and 1.6 g of triethylamine hydrochloride was heated at about 180° C. until no further ethanol was distilled out (for about 4 hours). The resulting mixture was then worked up in the same manner as described in Reference Example 2 (a) and the crystals thus obtained were recrystallized from chloroform-petroleum ether to obtain 25 g of 2,3-dihydro-3-ethoxycarbonyl-2-(p-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one as colorless needles having a melting point of 192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04264497 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-3a6c47db368f469694ed4994ce6f1e1b |
| Source note | uspto-grants-1981_04 |