HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → alpha-(4-Methoxybenzoyl)-alpha-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86741145 | HCID 86741145 | — |
| Reactant | HCID 178524450 | HCID 178524450 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | alpha-(4-Methoxybenzoyl)-alpha-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilide | HCID 86741146 | 93.3% |
Reaction Steps
33 g of α-chloro-α-(4-methoxybenzoyl)-2-chloro-5-dodecyloxycarbonylacetanilide and 16 g of 1-(4-carboxyphenyl)-5-mercaptotetrazole were dispersed in 200 ml of chloroform to which was added dropwise 10 ml of triethylamine at room temperature over a period of about 30 minutes. After stirring for 3 hours the chloroform solution was washed with water and concentrated under reduced pressure. The residue was recrystallized from methanol to obtain 41.2 g of α-(4-methoxybenzoyl)-α-[1-(4-carboxyphenyl)-5-tetrazolylthio]-2-chloro-5-dodecyloxycarbonylacetanilide. Yield: 93%. Melting Point: 172° to 174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628024 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-6fcad6eccd0d40518c24aeffb2ff0aa7 |
| Source note | uspto-grants-1986_12 |