HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-bromo-N-(2,4,6-trimethoxyphenyl)decanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,4,6-Trimethoxyaniline | HCID 84271 | — |
| Reactant | 2-Bromodecanoic acid | HCID 98310 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-bromo-N-(2,4,6-trimethoxyphenyl)decanamide | HCID 14995388 | 69.5% |
Reaction Steps
2-Bromodecanoic acid (1 g, 3.8 mmol) was heated under reflux in thionyl chloride (10 ml) for 1 hour. The thionyl chloride was evaporated and the residue was dissolved in dry ether (10 ml) and added dropwise to a solution of 2,4,6-trimethoxyaniline (0.7 g, 3.8 mmol) in pyridine (20 ml) at 0° C. and the mixture was stirred for 1.5 hours. The reaction mixture was poured into saturated aqueous ammonium chloride and extracted three times with ethyl acetate (60 ml). The combined organics were extracted with water and brine and dried and concentrated. Recrystallization from isopropyl ether afforded 1.1 g (65%) of the title compound, m.p. 109°-110° C. This material was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05362878 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-a039717299314874b89da6ba08f56f92 |
| Source note | uspto-grants-1994_11 |