HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1,2,3,4-Tetrahydro-6-hydroxy-7-methoxy-2-propionyl-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | 1,2,3,4-Tetrahydro-6-hydroxy-7-methoxy-isoquinoline-hydrochloride | HCID 24189397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2,3,4-Tetrahydro-6-hydroxy-7-methoxy-2-propionyl-isoquinoline | HCID 21447013 | 69.9% |
Reaction Steps
55.5 g of propionyl chloride are added dropwise at room temperature over a period of one hour to a mixture of 86.3 g of 1,2,3,4-tetrahydro-6-hydroxy-7-methoxy-isoquinoline-hydrochloride, 138,2 g of potassium carbonate, 600 ml of methylene chloride, and 480 ml of water. The mixture is stirred for an additional 18 hours, the organic phase is separated, and the aqueous phase is extracted twice with methylene chloride. The methylene chloride extracts are dried and evaporated. 65.8 g of 1,2,3,4-tetrahydro-6-hydroxy-7-methoxy-2-propionyl-isoquinoline are obtained. m.p. = 116° - 118° C. (ethyl acetate - diisopropyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013663 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-ddd7d265e0c144028128f0ea2938ee32 |
| Source note | uspto-grants-1977_03 |