HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → HCID 17603797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 17603797 | HCID 17603797 | — |
Reaction Steps
Alkylation of 3-hydroxybenzaldehyde with phenethyl bromide was done following the method used in Example 34, except that DMF was used as the reaction solvent, to give 3-phenethoxybenzaldehyde as a clear oil. Yield (0.98 g, 54%): 1H NMR (400 MHz, CDCl3) δ 9.96 (s, 1H), 7.21-7.48 (m, 8H), 7.18-7.20 (m, 1H), 4.24 (t, J=7.0 Hz, 2H), 3.13 (t, J=7.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07982071B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-6c5187d4b33f478d85e6358fb92e0673 |
| Source note | uspto-grants-2011_07 |