HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 53937757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Heptanoyl chloride | HCID 17313 | — |
| Product | HCID 53937757 | HCID 53937757 | 94% |
Reaction Steps
The procedure described in Example 1 is repeated, but in section a) aniline is used in place of n-pentylamine and n-heptanoyl chloride is used in place of caproyl chloride. N-Phenyl-n-heptenamide (m.p. 50° C.) is obtained in 94% yield. This is reacted with PCl5 as in Example 1, section b), and gives in quantitative yield N-phenyl-heptaneiminoyl chloride as a yellowish oil which is converted according to section c) into the desired product and purified by chromatography on silica gel in hexane/ether=1:1. M.p. 83°-84° C. UV (EtOH): 320 nm (ε=19502).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05481001 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-597761ed173644efa403721123336321 |
| Source note | uspto-grants-1996_01 |