HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Amino-1-ethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester | HCID 54323501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid Methyl Ester | HCID 14064723 | 66.4% |
Reaction Steps
To a solution of 4-amino-1-ethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester (6 g, 0.020 mol) in 50 mL THF was added 50 mL of H2O and paraformaldehyde (5 g) and the solution was heated at reflux for 2 hours under nitrogen. It was then cooled, concentrated in vacuo, and diluted with ethyl acetate. The ethyl acetate layer was washed with saturated sodium bicarbonate solution, brine, dried and concentrated in vacuo. The residue was purified by flash chromatography eluting with hexane to give a white solid (4 g, 66.4%) m.p. 86°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04748252 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-a6f2e00990214c2d94735a35b65b7d4c |
| Source note | uspto-grants-1988_05 |