HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5,6,7,8-Tetrahydro-8-hydroxy-4-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5,6,7,8-tetrahydro 4-methylquinoline-N-oxide | HCID 14835945 | — |
| Product | 5,6,7,8-Tetrahydro-8-hydroxy-4-methylquinoline | HCID 14835946 | — |
Reaction Steps
A solution of the crude product of Step 1 (19.2 g, 115 mmol) in acetic anhydride (100 ml) was heated at 110° for lh, cooled to room temperature, and evaporated in vacuo. The residue was dissolved in methanol (100 ml) and the solution treated with 4N-NaOH (100 ml). After 2h, the solution was concentrated in vacuo and the aqueous residue partitioned between dichloromethane (100 ml) and water (100 ml). The chlorinated phase was dried (Na2SO4), and evaporated in vacuo to give an oil which was purified by chromatography (silica; ether) to give the product as crystals (12.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075303 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-e34480a463d046248f3f6e3e77e662b7 |
| Source note | uspto-grants-1991_12 |