HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxy-5-nitrobenzyl alcohol → (2-Methoxy-5-nitrophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxy-5-nitrobenzyl alcohol | HCID 2763823 | — |
| Reactant | 2-Methoxy-5-nitrobenzaldehyde methyl hemiacetal | HCID 21014460 | — |
| Product | (2-Methoxy-5-nitrophenyl)methanol | HCID 17604241 | 76% |
Reaction Steps
This compound was prepared by reduction of 2-methoxy-5-nitrobenzaldehyde methyl hemiacetal using a method similar to that described for preparing 2-hydroxymethyl-4-nitrophenol in 76% yield: MP 121-122° C.; 1H NMR (DMSO-d6, 500 MHz) δ 8.22 (d, 1H, J=1.22 Hz), 8.16 (dd, 1H, J=2.7 and 9.1), 7.16 (d, 1H, J=8.9 Hz), 4.50 (s, 2H), 3.90 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07838542B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-cd09e21f39b946cbb35fba538315085e |
| Source note | uspto-grants-2010_11 |