HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 4-(2,3-Dihydroxypropoxy)-3-chlorobenzaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methyl morpholine oxide | HCID 82029 | — |
| Edukt | 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde | HCID 4770036 | — |
| Katalysator | tert-Butanol | HCID 6386 | — |
| Katalysator | Osmium Tetroxide | HCID 30318 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-(2,3-Dihydroxypropoxy)-3-chlorobenzaldehyde | HCID 79839648 | — |
Reaktionsschritte
The above 4-allyloxy-3-chloro-benzaldehyde (5.37 g, 27.3 mmol) is dissolved in acetone (100 mL) and water (10 mL) and treated with a 2.5% solution of OsO4 in tert.-butanol (1.71 mL, 0.137 mmol OsO4). N-methyl morpholine-N-oxide (3.87 g, 32.8 mmol) is added and the reaction mixture is stirred at rt for 20 h before it is diluted with EA (300 mL) and washed with 10% aq. citric acid solution (200 mL) and water (2×150 mL). The washings are extracted with EA (300 mL) and the combined organic extracts are dried over MgSO4, filtered and concentrated to furnish the title compound (6.02 g) as beige foam which was used in the following steps without further purification. LC: tR=0.67 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08524752B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-a50a026ccdeb406389225a2375678e72 |
| Quellennotiz | uspto-grants-2013_09 |