HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1153719Erstellt: 26. Oktober 2026
Dichloromethane → 3-(Dodecane-1-sulfonyl)-2-(nitromethylidene)-1,3-thiazinane
https://huagongshe.com/reaction/1153719
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 2-nitromethylenetetrahydro-2H-1,3-thiazine | HCID 42853 | — |
| Edukt | Dodecylsulfonyl chloride | HCID 66280 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-(Dodecane-1-sulfonyl)-2-(nitromethylidene)-1,3-thiazinane | HCID 53912032 | — |
Reaktionsschritte
1.6 g of 2-(nitromethylene)-tetrahydro-2H-1,3-thiazine, 3.18 g of ethyldiisopropylamine and 20 ml of methylene chloride were mixed. The mixture was cooled to and stirred at -60° C. under a nitrogen atmosphere while 2.95 g of dodecanesulfonyl chloride was added in portions over a 10 minute period. The mixture was allowed to warm to 10° C. (2.5 hours), then stirred at 10° C. for 1 hour and at 20° C. for 1.5 hours. The resulting mixture was poured into water, and the organic phase was separated, dried (MgSO4), filtered and stripped of solvent. The residue, a gum, was chromatographed over silica gel, using methylene chloride as eluent. After workup the product was recrystallized from ethanol to give N-(dodecylsulfonyl)-2-(nitromethylene)-tetrahydro-2H-1,3-thiazine (3A) as a solid, m.p.: 116°-117° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04486427 |
|---|
| Quelldatensatz | uspto-grants-1984_12 |
|---|
| ORD ID | ord-b1afed8fd099419786edb1cc6b2f27d9 |
|---|
| Quellennotiz | uspto-grants-1984_12 |
|---|