HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 411973Erstellt: 23. Oktober 2026
Triethylamine → [[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid
https://huagongshe.com/de/reaction/411973
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Benzhydryl isothiocyanate | HCID 520742 | — |
| Edukt | N-methyl aminooxy acetic acid hydrochloride | HCID 85852466 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | [[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid | HCID 12045032 | 93,7% |
Reaktionsschritte
A mixture of benzhydryl-isothiocyanate (13.75 g), N-methyl aminooxy acetic acid hydrochloride (8.6 g), triethylamine (16 g) and chloroform (200 mL) was heated at reflux for three hours, stirred at ambient temperature for one hour. The mixture was diluted with chloroform (200 mL) and washed with 2N HCl (2×300 mL) then with water (300 mL). The organic phase was dried over anhydrous magnesium sulfate and evaporated to dryness to give a solid. The solid was stirred in ether (200 mL) and filtered to give 18.8 g of [[[[(benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid as a white solid, m.p. 160-162° C. Mass spectrum (−FAB, [M−H]−) m/z 329. 1H-NMR (DMSO-d6; 400 MHz) δ13.55 (br s, 1H), 9.75 (d, 1H), 7.35-7.23 (m, 10H), 6.63 (d, 1H), 4.63 (s, 2H), and 3.42 ppm (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06562814B2 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-50183eaf6cae4780bfbc10c19dadfbdb |
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| Quellennotiz | uspto-grants-2003_05 |
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