HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → HCID 20133036, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | HCID 3798338 | HCID 3798338 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20133036 | HCID 20133036 | — |
Reaction Steps
By procedures described in Example 1 (Method A), phenethylamine and propionyl chloride were converted to 1-ethyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 2.5 g of this isoquinoline compound in 50 ml toluene. With this mixture stirred, 1.5 ml dichloroacetyl chloride was added dropwise to the mixture. The mixture was refluxed until a clear solution appeared. The mixture was stripped of solvent and subjected to Kugelrohr distillation (150° C. @ 0.25 mm Hg) to provide 2.7 g of product having the elemental analysis reported in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755218 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-d15e90395e194ec0b8ded4610d4128fb |
| Source note | uspto-grants-1988_07 |