HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585098Generated: November 1, 2026
Methyl iodide → 2-(Methylamino)-4-nitrophenol
https://huagongshe.com/reaction/1585098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-Nitrophenol | HCID 3613389 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Methylamino)-4-nitrophenol | HCID 21221759 | — |
Reaction Steps
Triethylamine (2 ml, 14.4 mmol) was added to a solution of 2-amino-4-nitrophenol (1) (1.54 g, 10 mmol) and methyl iodide (1 ml, 16 mmol) in methanol (10 ml). After 1 hour at 40° C., further methyl iodide (1 ml) and triethylamine (1 ml) were added and the mixture was stirred at 40° C. for a further 2 hours. The reaction mixture was concentrated to dryness in vacuo, the residue was added to aqueous 2N sodium acetate solution and the mixture was extracted with ethyl acetate. The organic phase was dried with sodium sulfate and chromatographed on silica gel (eluent dichloromethane/methanol 95/5). Yield 880 mg (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05935995 |
|---|
| Source dataset | uspto-grants-1999_08 |
|---|
| ORD ID | ord-66aae1aa20a84164b9801f127695ea82 |
|---|
| Source note | uspto-grants-1999_08 |
|---|