HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → HCID 20133037, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trifluoroacetyl chloride | HCID 61106 | — |
| Reactant | 113721-77-0 | HCID 21476433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20133037 | HCID 20133037 | — |
Reaction Steps
By procedures described in Example 1 (Method A), phenethylamine and trifluoroacetyl chloride were converted to 1-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 3.5 g of this isoquinoline compound, 20 ml 10% sodium hydroxide and 50 ml methylene chloride. With this mixture stirred, 2 ml dichloroacetyl chloride was added dropwise to the mixture. The mixture was stirred for 2 minutes, then water was added. The organic extract was dried with magnesium sulfate, stripped of solvent, and subjected to Kugelrohr distillation (130° C. @ 0.1 mm Hg) to provide a 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-5ce56d7639d64677b75a570b2da00412 |
| Source note | uspto-grants-1988_07 |