HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Reactant | 4-Chloro-3-methoxy-2-methylpyridine | HCID 10583046 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine | HCID 15279358 | — |
Reaction Steps
16 g of 4-chloro-3-methoxy-2-methylpyridine, 63 g of phenol and 40 g of O-benzylhydroxylamine are stirred at 120° C. under nitrogen for 4 hours. After cooling, the mixture is shaken with 500 ml of 2N NaOH and CH2Cl2. The aqueous phase is extracted a second time with CH2Cl2. After concentrating the combined CH2Cl2 phases, excess O-benzylhydroxylamine is distilled off in vacuo at 0.6 mm. The residue crystallizes on stirring with hexane. After filtering off with suction and washing with hexane 21.6 g=88.4% of product remain. The product is recrystallized from ethyl acetate. M.p.: 130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723450 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-5d39e4809233431997c0a9624f5079c5 |
| Source note | uspto-grants-1998_03 |