HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 2,4,5-Trimethoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,2,4-Trimethoxy-5-nitrobenzene | HCID 822415 | — |
| Reactant | Tin tetrachloride dihydrate | HCID 85782573 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,4,5-Trimethoxyaniline | HCID 12410138 | 54.3% |
Reaction Steps
1,2,4-Trimethoxy-5-nitro-benzene (1.20 g, 5.63 mmol) and tin chloride dihydrate (3.81 g, 16.9 mmol) in ethyl acetate (50 mL) was stirred at 65-70° C. for 20 h. The reaction was cooled, carefully neutralized with sodium bicarbonate and was filtered through Celite. The organic phase was washed with brine, dried (sodium sulfate) and was evaporated. Purification by flash chromatography (SiO2) eluted with 3:7 ethyl acetate:hexanes provided 2,4,5-trimethoxy-phenylamine (0.56 g, 54% yield) as a tan solid. 1H-NMR (DMSO-d6, 500 MHz) 6.57 (s, 1H), 6.37 (s, 1H), 3.70 (s, 3H), 3.65 (s, 3H), 3.63 (s, 3H) ppm; HPLC (Method A) 2.163 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902239B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-a6b536d91ec94f6fbd89326ad637e0d7 |
| Source note | uspto-grants-2011_03 |