HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Piperidinecarboxaldehyde → 10-Hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | 10-Hexyl-3,7-dimethoxy-phenothiazine | HCID 18972496 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ether tetrahydrofuran | HCID 21868444 | — |
| Product | 10-Hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehyde | HCID 18972606 | 64.4% |
Reaction Steps
A solution of 3.42 g (10.0 mmol) of 10-hexyl-3,7-dimethoxy-phenothiazine in 50 ml of diethyl ether/tetrahydrofuran (4:1) was reacted with 8.12 ml of n-butyllithium solution (1.6M in hexane) and 3.35 g (29.6 mmol) of N-formylpiperidine analogously to that described in Example 4.1.1.c. The product was chromatographed on silica gel with ethyl acetate/hexane (1:4), whereupon 2.39 g (64.4%) of 10-hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehyde were obtained as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811389 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-b79ee955c69b4f9383b50c2ddf80b2a8 |
| Source note | uspto-grants-1998_09 |