HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268774Generated: October 31, 2026
Dimethylmalonic acid → N-(4-methylthiophenyl)-2,2-dimethylmalonamic acid
https://huagongshe.com/reaction/2268774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylmalonic acid | HCID 11686 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Methylthio)aniline | HCID 66038 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-methylthiophenyl)-2,2-dimethylmalonamic acid | HCID 53858939 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329366B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-743e6761e7fd42b3a433e12ce3be0afc |
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| Source note | uspto-grants-2001_12 |
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