HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1760522Erstellt: 27. Oktober 2026
Dimethylmalonic acid → N-(4-methylthiophenyl)-2,2-dimethylmalonamic acid
https://huagongshe.com/reaction/1760522
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylmalonic acid | HCID 11686 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 4-(Methylthio)aniline | HCID 66038 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(4-methylthiophenyl)-2,2-dimethylmalonamic acid | HCID 53858939 | — |
Reaktionsschritte
Thionyl chloride (8.15 g, 5 ml, 0.069 mol) was added to a stirred solution of 2,2-dimethylmalonic acid (7.26 g, 0.055 mol) in dry THF (55 ml). The mixture was heated under reflux for 3 hr. The reaction mixture was cooled to room temperature and 4-methylthioaniline (15.3 g, 0.11 mol) in THF (30 ml) was then added dropwise over 30 mins to the solution. The mixture was stirred at room temperature for 2 hr. The reaction mixture was then concentrated in vacuo and then treated with hydrochloric acid (2N, 100 ml). The product was extracted with ethyl acetate (2×100 ml). The organic extracts were combined, then washed with water (100 ml) and saturated sodium hydrogen carbonate solution (5×80 ml). The organic layer was then acidified with hydrochloric acid (5N, 250 ml) and the resultant white crystalline precipitate was collected by filtration to afford N-(4-methylthiophenyl)-2,2-dimethylmalonamic acid. mp 130-132° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06844338B2 |
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| Quelldatensatz | uspto-grants-2005_01 |
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| ORD ID | ord-46c241adb70544f493479d5acc0f2e7b |
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| Quellennotiz | uspto-grants-2005_01 |
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