HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 728428Erstellt: 25. Oktober 2026
Triethylamine → 3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane
https://huagongshe.com/reaction/728428
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Chlorobutane-1-sulphonyl chloride | HCID 74212 | — |
| Edukt | 2-Methoxy-3-octadecylcarbamoyloxypropylamine | HCID 14992262 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane | HCID 14835031 | 77% |
Reaktionsschritte
To a solution of 1.2 g (3 mM) of 2-methoxy-3-octadecylcarbamoyloxypropylamine IVa1 in 24 ml of dichloromethane and 0.5 ml (3.6 mM) of triethylamine is added 0.75 g (3.93 mM) of 4-chlorobutanesulfonyl chloride with ice-cooling and the mixture is stirred at room temperature overnight. The product is isolated with dichloromethane extraction and dichloromethane layer is washed with saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and evaporated. The residue is purified by the column chromatography on silica gel with a n-hexane-ethyl acetate (3:2) mixture as an eluent. The product is recrystallized from dichloromethane-n-hexane to give 1.28 g (2.305 mM) of 3-(4-chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane IIIa5 as colorless crystals in 77% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05047540 |
|---|
| Quelldatensatz | uspto-grants-1991_09 |
|---|
| ORD ID | ord-3eaddd452a6a4961beaa3b84ccbf49b8 |
|---|
| Quellennotiz | uspto-grants-1991_09 |
|---|