HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Methoxy-2-capryloyl-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-Methoxy-1,2,3,4-tetrahydroisoquinoline | HCID 39356 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Methoxy-2-capryloyl-1,2,3,4-tetrahydroisoquinoline | HCID 20155809 | — |
Reaction Steps
4.0 g of 6-methoxy-1,2,3,4-tetrahydroisoquinoline and 3.5 ml of triethylamine in 50 ml of methylene chloride are initially introduced, and a solution of 4.0 g of octanoyl chloride in 10 ml of methylene chloride is added dropwise with stirring and cooling. The mixture is stirred at room temperature for 1 hour, then shaken with 1N hydrochloric acid, sodium carbonate solution and water, and the organic phase is dried over magnesium sulfate and evaporated in a rotary evaporator. The crude product (6.7 g of colorless oil) is reacted further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04717724 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-4634ee63f25b4374b64a956d86e950da |
| Source note | uspto-grants-1988_01 |