HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-Acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 21447025 | HCID 21447025 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline | HCID 21447007 | 79.9% |
Reaction Steps
A mixture of 122.3 g of 5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline-hydrochloride, 36.1 g of sodium acetate, 81.7 g of acetic anhydride, and 500 ml of methylene chloride is stirred for 1 hour at the boiling point. After cooling, the mixture is combined with 500 ml of water and the organic phase is separated and evaporated to dryness under reduced pressure. 99.5 g of 2-acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline are obtained. m.p. = 94° - 95° 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-955f010b617943459fe35ffb7051e9cf |
| Source note | uspto-grants-1977_03 |