HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isovanillin → HCID 59333870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isovanillin | HCID 12127 | — |
| Reactant | HCID 11097066 | HCID 11097066 | — |
| Product | HCID 59333870 | HCID 59333870 | 57% |
Reaction Steps
Isovanillin (0.78 g, 5.2 mmol) was alkylated using hex-5-ynyl 4-methylbenzenesulfonate (1.95 g, 7.73 mmol according to Procedure 4. The crude product was recystallised from EtOAc/petrol to provide 3-(hex-5-ynyloxy)-4-methoxybenzaldehyde (0.68 g, 57%) as a colourless crystalline solid; mp 66-67° C.; δH (400 MHz, CDCl3) 1.74 (p, J=7.2 Hz, 2H, CH2), 1.96-2.0 (m, 3H, CH2, C≡CH), 2.30 (td, J=7.2, 2.8 Hz, 2H, CH2C≡CH), 3.95 (s, 3H, OCH3), 4.11 (t, J=7.2 Hz, 2H, OCH2), 6.97 (d, J5,6=8.0 Hz, 1H, H5), 7.40 (d, J2,6=1.6 Hz, 1H, H2), 7.44 (dd, J5,6=8.0 Hz, J2,6=1.6 Hz, 1H, H6), 9.84 (s, 1H, CHO); δC (100 MHz, CDCl3) 18.1, 25.0, 28.0, 56.2, 68.4, 68.7, 83.9, 110.3, 110.6, 126.7, 130.1, 149.0, 154.9, 190.9; vmax 1018, 1263, 1582, 1679, 2933, 3238 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765812B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-35e7f64476604296a2d3366c2f3c1459 |
| Source note | uspto-grants-2014_07 |