HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octyne → HCID 20147164, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octyne | HCID 12370 | — |
| Reactant | 4-Bromothiophene-2-carbaldehyde | HCID 87792 | — |
| Product | HCID 20147164 | HCID 20147164 | 89% |
Reaction Steps
Reaction of 4-bromo-2-thiophenecarboxaldehyde (3.40 g 2 mmole, prepared by the methods described by D. Chadwick et al, J.C.S. Per 1 1766, 1973), with 1-octyne (4.40 g, 4 mmole) as described in Example 20 gave the title compound as a yellow oil (89.0%); mp 2° C.; νmax 3100, 2260, 1685, 1160, 855, 655, 622; δH(CDCl3) 0.88(3H, t, J=6 Hz), 1.3(8H, m), 2.33(2H, t, J=6 Hz), 7.7(2H, s), 9.9 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04732901 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-8fb0565ec0564f4a8089b45f4297a6d1 |
| Source note | uspto-grants-1988_03 |