HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14054322, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | HCID 14054310 | HCID 14054310 | — |
| Reactant | HCID 21273355 | HCID 21273355 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 14054322 | HCID 14054322 | — |
Reaction Steps
The reaction is carried out as in Example 1, starting with 7-phenylbenzo[b]thiophene-5-carboxylic acid (3 g) in toluene (30 cc) and thionyl chloride (2.64 cc) and then triethylamine (5 cc) and N-methylethylamine (1.01 cc) in toluene (30 cc). After chromatography of the residue on silica gel using a cyclohexane:ethanol:ethyl acetate (90:5:5 by volume) mixture as the eluent, a residue is obtained, which is stirred overnight in 40°-60° petroleum spirit (50 cc). After filtering and drying, N-ethyl-N-methyl-7-phenylbenzo[b]thiophene-5-carboxamide (1.5 g), m.p. 93° C., is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808599 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-ffc24fbc8d5e4b8faacd72db18470ca8 |
| Source note | uspto-grants-1989_02 |