HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexadecane → HCID 178516453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | HCID 788030 | HCID 788030 | — |
| Reactant | HCID 22753008 | HCID 22753008 | — |
| Reactant | HCID 22753015 | HCID 22753015 | — |
| Product | HCID 178516453 | HCID 178516453 | 51.6% |
Reaction Steps
Using 11.6 g of 2,4-dichloro-5-(4-nitrophenoxy)-aniline hydrochloride and 13.1 g of 1-(2,4,6-trichlorophenyl)-3-ethoxy-2-pyrazolin-5-one, which were prepared in a manner similar to Steps (1) and (2) of Synthesis Example 1 except that 21.2 g of 4-fluoronitrobenzene was used in lieu of hexadecyl bromide in Step (1) of Synthesis Example 1, procedures similar to Step (3) of Synthesis Example 1 were carried out. In this case, 10.0 g of the desired product was obtained without recrystallization. The melting point thereof was 305 to 306° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04133686 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-e38f141859fa4169a68a4028ab8dcaab |
| Source note | uspto-grants-1979_01 |