HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 20133049, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | 2-Phenylpropylamine | HCID 11398 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloropropionyl chloride | HCID 111019 | — |
| Reactant | 4-Methyl-1,2,3,4-tetrahydroisoquinoline | HCID 13738934 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20133049 | HCID 20133049 | — |
Reaction Steps
By procedures described in Example 1 (Method A), β-methyl-phenethylamine and benzoyl chloride were converted to 4-methyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 4.0 g of this isoquinoline compound, 10 ml 10% sodium hydroxide and 50 ml methylene chloride. With this mixture stirred, 2 ml 2-chloropropionyl chloride was added dropwise to the mixture. The mixture was stirred for 15 minutes, then water was added. The organic extract was dried with magnesium sulfate, stripped of solvent and subjected to Kugelrohr distillation (150° 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-616c0c6a40004da1b5cd33478a9fbaed |
| Source note | uspto-grants-1988_07 |