HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dimethyl-6-nitrobenzenemethanol → 2,3-Dimethyl-6-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dimethyl-6-nitrobenzenemethanol | HCID 13937016 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dimethyl-6-nitrobenzaldehyde | HCID 13937020 | 93.3% |
Reaction Steps
A solution of 2,3-dimethyl-6-nitrobenzenemethanol (34.88 g, 0.192 mole) in dichloromethane (150 mL) was added to a stirred mixture of pyridinium chlorochromate (62.2 g, 0.288 mole) in dichloromethane (250 ml). The mixture was stirred vigorously for 4 hours, diluted with diethyl ether (500 mL) and the organic layer decanted. The residue was washed with diethyl ether (500 mL) and the combined organic solution filtered through a plug of silica gel (6"×11/2"). Evaporation of the solvent afforded 2,3-dimethyl-6-nitrobenzaldehyde (32.08 g, 93%). An analytical sample was prepared by crystallizing from diisopropyl ether and had m.p. 66°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04668686 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-6899a719a9724c8dacf0fd3cc7f5d83a |
| Source note | uspto-grants-1987_05 |