HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 54101020, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13579990 | HCID 13579990 | — |
| Product | HCID 54101020 | HCID 54101020 | — |
Reaction Steps
A solution of 5,6,7,8-tetrahydro-2-methyl-3-quinolinecarboxylic acid ethyl ester (2.19 g) and 4-hydroxybenzaldehyde (1.32 g, 11 mmol) in acetic anhydride (6.5 ml) is heated at reflux temperature for 18 hours. The solution is evaporated, the residue dissolved in tetrahydrofuran and crude 8-[[4-(acetyloxy)phenyl)methylene]-5,6,7,8-tetrahydro-2-methyl-3-quinolinecarboxylic acid ethyl ester is precipitated with water to yield 3.4 g. Purification on silica gel (250 g) with 9:1 Skelly B:ethyl acetate gives pure 8-[[4-(acetyloxy)phenyl)-methylene]-5,6,7,8-tetrahydro-2-methyl-3-quinolinecarboxylic acid ethyl ester (2.76 g), m.p. 112° C., after ethanol crystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576949 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-25203c70e36f4b52bb76e7fe3277e277 |
| Source note | uspto-grants-1986_03 |