HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → HCID 14054340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13637983 | HCID 13637983 | — |
| Reactant | Cyclohexane ethylacetate | HCID 21867204 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 14054340 | HCID 14054340 | — |
Reaction Steps
The reaction is carried out as in Example 1, starting with 4-(4-chlorophenyl)benzo[b]thiophene-6-carboxylic acid (4.67 g) in toluene (45 cc) and thionyl chloride (3.6 cc) and then triethylamine (6.9 cc) and diethylamine (1.7 cc) in toluene (45 cc). After chromatography of the residue using a cyclohexane:ethyl acetate (90:10 by volume) mixture as the eluent, a residue is obtained, which is stirred for 2 hours in 40°-60° petroleum spirit. After filtering and drying, N,N-diethyl-4-(4-chlorophenyl)benzo[b]thiophene-6-carboxamide (1.07 g), m.p. 135° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808599 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-d64db60bf82f4973b80e9e726e39336d |
| Source note | uspto-grants-1989_02 |