HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Dimethylamino-1-naphthaldehyde → (E)-2-[2-(4-dimethylaminonaphthalen-1-yl)vinyl]-3-heptylbenzothiazol-3-ium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Dimethylamino-1-naphthaldehyde | HCID 608052 | — |
| Reactant | 3-Heptyl-2-methylbenzothiazolium iodide | HCID 67572016 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | (E)-2-[2-(4-dimethylaminonaphthalen-1-yl)vinyl]-3-heptylbenzothiazol-3-ium iodide | HCID 67571245 | — |
Reaction Steps
A mixture of 3-heptyl-2-methylbenzothiazolium iodide (0.50 g, 1.33 mmol) and 4-dimethylamino-1-naphthaldehyde (0.40 g, 2.01 mmol) in 5 mL of acetic anhydride under nitrogen was heated. Upon refluxing, the mixture turned purple and all solids seemed to be in solution. The solution was refluxed for 15 minutes and on cooling, solid formed. The mixture was filtered and washed with ethyl acetate to give (E)-2-[2-(4-dimethylaminonaphthalen-1-yl)vinyl]-3-heptylbenzothiazol-3-ium iodide as a dark brown solid, mp 195-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001331 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-e3e481c3262c42168acfaec6390db418 |
| Source note | uspto-grants-1999_12 |