HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → HCID 20147153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | HCID 20147157 | HCID 20147157 | — |
| Product | HCID 20147153 | HCID 20147153 | 96.7% |
Reaction Steps
Reaction of 5-(1-octynyl)-2-thiophenecarboxaldehyde (2.64 g 12 mmole) with diethyl malonate as described in Example 3 yielded the title compound as a yellow oil 4.2 g (96.7%). νmax (film) 2225, 1730, 1615, 865, 805; δ(CDCl3), 0.90(3H, t, J=6 Hz), 1.5(14H, m), 2.32(2H, t, J=6 Hz), 4.30(2H, q, J=7.5), 4.4(2H, q, J=7.5), 7.03 (1H, d, J=3 Hz), 7.23(1H, d, J=3 Hz), 7.76(1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04732901 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-1a9670d19726497fb65c0d1bf0930e68 |
| Source note | uspto-grants-1988_03 |