HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → HCID 178436623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-(4-Cyano-2-ethyl-6-methylphenyl)propionic acid | HCID 57437414 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178436623 | HCID 178436623 | 81.1% |
Reaction Steps
Potassium tert.butoxide (2.71 g, 24.1 mmol) is carefully dissolved in methanol (25 mL). To this solution hydroxylamine hydrochloride (1.44 g, 20.7 mmol) followed by 3-(4-cyano-2-ethyl-6-methyl-phenyl)-propionic acid (1.50 g, 6.90 mmol) dissolved in methanol (7.5 mL) is added. The mixture is refluxed for 8 h and the solvent is evaporated. The residue is dissolved in 2 N aq. HCl and extracted with EA. The pH of the aq. phase is adjusted to pH 5 by adding sat. aq. NaHCO3 and the mixture is extracted three times with EA. The combined organic extracts are dried over Na2SO4, filtered, evaporated and dried to give 3-[2-ethyl-4-(N-hydroxycarbamimidoyl)-6-methyl-phenyl]-propionic acid (1.4 g) as a white solid; LC-MS: tR=0.60 min, [M+1]+=251.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039644B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-2996159b3b2841079b77fdd563614c01 |
| Source note | uspto-grants-2011_10 |