HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 178467950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(2,2-diethoxyethyl)carbodiimide | HCID 10749464 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178467950 | HCID 178467950 | 73.8% |
Reaction Steps
Aniline (1.66 g, 17.8 mmol) was dissolved in ethanol (25 mL), and N-(2,2-diethoxyethyl)carbodiimide (a), (2.82 g, 17.8 mmol), was added dropwise. Then methanesulfonic acid (1.71 g, 17.8 mmol) was added, and the mixture was warmed at reflux for 24 h. The reaction mixture was poured into NaOH (0.5 M) and extracted with CH2Cl2. Drying and concentration afforded a product that was subjected to flash chromatography to give the intermediate guanidine (b) (3.3 g, 73.8%). NMR (500 MHz, DMSO-d6) δ 7.27-6.90 (m, 5H), 4.55 (t, 1H), 3.76-3.70 (m, 2H), 3.60-3.54 (m, 2H), 3.35-3.34 (d, 2H), 1.22 (pent, 6H). MS: 249.8 (M−H)−; 252.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822513B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-bd4e889ec77b4ab59013856aa493297f |
| Source note | uspto-grants-2014_09 |