HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzaldehyde → Ethyl 3-(3-formylphenyl)but-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Reactant | Ethyl trans-crotonate | HCID 429065 | — |
| Product | Ethyl 3-(3-formylphenyl)but-2-enoate | HCID 86632145 | — |
Reaction Steps
Coupling of 3 bromobenzaldehyde with ethyl crotonate following the method used in Example 26 gave ethyl 3-(3-formylphenyl)but-2-enoate as a light yellow oil Yield (0.547, 23%): 1H NMR (300 MHz, CDCl3) δ 10.05 (s, 1H), 7.99 (t, J=1.6 Hz, 1H), 7.87 (dt, J=7.6, 1.3 Hz, 1H), 7.74 (m, 1H), 7.56 (t, J=7.6 Hz, 1H), 6.19 (q, J=1.2 Hz, 1H), 4.23 (q, J=7.2 Hz, 2H), 2.61 (d, J=1.2 Hz, 3H), 1.33 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09314467B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-8836aa34becb4d87ab276facbf2eace2 |
| Source note | uspto-grants-2016_04 |