HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Chloro-3-hydroxy-5-nitro-p-anisaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetate | HCID 14450994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Chloro-3-hydroxy-5-nitro-p-anisaldehyde | HCID 14450995 | — |
Reaction Steps
35.8 g of 2-chloro-3-formyl-6-methoxy-5-nitrophenyl acetate are dissolved in 300 ml of methanol. After adding 145 ml of 1N sodium hydroxide solution the mixture is stirred at 23° for 1 hour. After evaporation of the methanol, the residue is diluted with ice-water, made acid with 2N hydrochloric acid and extracted twice with 400 ml of ethyl acetate each time. The organic phases are washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated. The residue is recrystallized from methylene chloride/petroleum ether. There is obtained 2-chloro-3-hydroxy-5-nitro-p-anisaldehyde of m.p. 130°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633371 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-04542192903b4a61b15fae02838c30bf |
| Source note | uspto-grants-1997_05 |