HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178436623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-(4-Cyano-2-ethyl-6-methylphenyl)propionic acid | HCID 57437414 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178436623 | HCID 178436623 | 101.6% |
Reaction Steps
To a solution of 3-(4-cyano-2-ethyl-6-methyl-phenyl)-propionic acid (10.0 g, 46.0 mmol) in EtOH (80 mL), NEt3 (13.97 g, 138.1 mmol) followed by hydroxylamine hydrochloride (6.40 g, 92.1 mmol) is added. The mixture is refluxed for 7 h before it is cooled to rt. The solvent is removed in vacuo. The residue is dissolved in 2 N aq. HCl and the pH is adjusted to 5 by adding 32% aq. NaOH solution. The precipitate that forms is collected, washed with water and dried under high vacuum at 40° C. for 18 h to give 3-[2-ethyl-4-(N-hydroxycarbamimidoyl)-6-methyl-phenyl]-propionic acid (11.7 g) as a beige crystalline powder; LC-MS: tR=0.60 min, [M+1]+=251.09.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288554B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-e3a5cf88dcae4e0d86562675fc92a00d |
| Source note | uspto-grants-2012_10 |