HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-isobutyl acetamidotriphenylphosphonium chloride → N-isobutyl 7-thienyl-(2E)-hepten-6-ynamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-isobutyl acetamidotriphenylphosphonium chloride | HCID 23049290 | — |
| Reactant | 5-Thienyl-4-pentyn-1-al | HCID 54442563 | — |
| Product | N-isobutyl 7-thienyl-(2E)-hepten-6-ynamide | HCID 23049307 | — |
Reaction Steps
N-isobutyl 7-thienyl-(2E)-hepten-6-ynamide was prepared from 5-thienyl-4-pentyn-1-al and N-isobutyl acetamidotriphenyl-phosphonium chloride as in Example 9 and then converted to the title product by semihydrogenation as in Example 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855086 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-5ae2c3d2f8664f34bc84eb5f647d4705 |
| Source note | uspto-grants-1989_08 |