HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Cyclohexylmethoxy)aniline → HCID 22417939, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Cyclohexylmethoxy)aniline | HCID 15681651 | — |
| Reactant | Ethyl 4-chloroquinoline-6-carboxylate | HCID 22417892 | — |
| Product | HCID 22417939 | HCID 22417939 | — |
Reaction Steps
In a manner similar to that described in Example 39, Part B., 2.0 g (8.48 mmol) of ethyl 4-chloroquinolin-6-carboxylate and 1.74 g (8.48 mmol) of 4-(cyclohexylmethyloxy)aniline were transformed into the title compound: yield 3.41 g (92%); m.p. 251°-253° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05506235 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-b9bbafaa82e64ba188808bf816c2f825 |
| Source note | uspto-grants-1996_04 |