Matches in SemOpenAlex for { <https://semopenalex.org/work/W1946831239> ?p ?o ?g. }
- W1946831239 abstract "(1; R = Me)[18871-66-4] C6H15NO2 (MW 133.19)InChI = 1S/C6H15NO2/c1-6(8-4,9-5)7(2)3/h1-5H3InChIKey = FBZVZUSVGKOWHG-UHFFFAOYSA-N(2; R = Me)[867-89-0] C5H11NO (MW 101.15)InChI = 1S/C5H11NO/c1-5(7-4)6(2)3/h1H2,2-4H3InChIKey = JTZFZDSUVLTEHV-UHFFFAOYSA-N(3; R = Et)[19429-85-7] C8H19NO2 (MW 161.24)InChI = 1S/C8H19NO2/c1-6-10-8(3,9(4)5)11-7-2/h6-7H2,1-5H3InChIKey = XUFDMPZZAIRCGV-UHFFFAOYSA-N(4; R = Et)[816-65-9] C6H13NO (MW 115.17)InChI = 1S/C6H13NO/c1-5-8-6(2)7(3)4/h2,5H2,1,3-4H3InChIKey = BQGJNCWENLLBSP-UHFFFAOYSA-N(Eschenmoser–Claisen rearrangements;2 monoacylation of diols;3 triazine synthesis4)Physical Data: mixture of (1) and (2) bp 105–110 °C; d 0.911 g cm−3. Mixture of (3) and (4) bp 126–129 °C. (2) bp 104–105 °C. (4) bp 126 °C.Solubility: sol benzene, toluene, xylene, DMF, chloroform.Form Supplied in: amide acetal (1) is commercially available, usually as a mixture of (1) and (2). The commercial mixture is 85–95% pure; methanol (5–10%) may be present as a stabilizer.Preparative Method: O-methylation of N,N-dimethylacetamide with Dimethyl Sulfate (or diethyl sulfate), followed by reaction with Sodium Methoxide (or ethoxide). Fractional distillation affords mixtures of (1) and (2) (or 3 and 4). Treatment with calcium metal and redistillation gives the ketene O,N-acetals (2) (58%) (or 4; 74%).5" @default.
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- W1946831239 date "2009-03-15" @default.
- W1946831239 modified "2023-09-26" @default.
- W1946831239 title "N,N-Dimethylacetamide Dimethyl Acetal" @default.
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- W1946831239 doi "https://doi.org/10.1002/047084289x.rd293.pub2" @default.
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