HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxy-5-nitrobenzyl alcohol → (5-Nitro-2-propoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxy-5-nitrobenzyl alcohol | HCID 2763823 | — |
| Reactant | 5-Nitro-2-propyloxybenzaldehyde | HCID 21904357 | — |
| Product | (5-Nitro-2-propoxyphenyl)methanol | HCID 21904358 | 93% |
Reaction Steps
This compound was prepared by reduction of 5-nitro-2-propyloxybenzaldehyde using a method similar to that described for preparing 2-hydroxymethyl-4-nitrophenol in 93% yield: MP (No Sample left for MP); 1H NMR (400 MHz, DMSO-d6) 8.22 (d, 1H, J=2.6 Hz), 8.13 (dd, 1H, J=2.9 and 9.2 Hz), 7.14 (d, 1H, J=9.2 Hz), 5.41 (t, 1H, J=5.5 Hz), 4.52 (d, 2H, J=5.8 Hz), 4.08 (t, 2H, J=6.2), 1.75 (m, 2H), 0.98 (t, 3H, J=7.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07427608B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-c45ef040129c4864b721401ad67706bb |
| Source note | uspto-grants-2008_09 |