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Chemical Structure| 13831-32-8 Chemical Structure| 13831-32-8

Structure of 13831-32-8

Chemical Structure| 13831-32-8

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Product Details of [ 13831-32-8 ]

CAS No. :13831-32-8
Formula : C5H9NO3
M.W : 131.13
SMILES Code : CC(OCNC(C)=O)=O

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Application In Synthesis of [ 13831-32-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 13831-32-8 ]

[ 13831-32-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 625-51-4 ]
  • [ 13831-32-8 ]
YieldReaction ConditionsOperation in experiment
With pyridine; acetic anhydride; In 5,5-dimethyl-1,3-cyclohexadiene; EXAMPLE 11 Preparation of <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> acetate (ester) STR24 Acetic anhydride (25 g) and pyridine (10 drops) is added to <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> (9 g, 0.1 mol). The reaction mixture is stirred overnight at room temperature, concentrated in vacuo and chased with xylene to give the title product as an oil (11.9 g, 0.9 mol) which is identified by 1 H-NMR spectral analysis.
With pyridine; In 5,5-dimethyl-1,3-cyclohexadiene; EXAMPLE 11 Preparation of <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> acetate (ester) STR27 Acetic anhydrive (25 g) and pyridine (10 drops) is added to <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> (9 g, 0.1 mol). The reaction mixture is stirred overnight at room temperature, concentrated in vacuo and chased with xylene to give the title product as an oil (11.9 g, 0.9 mol) which is identified by 1 H-NMR spectral analysis.
With pyridine; acetic anhydride; In 5,5-dimethyl-1,3-cyclohexadiene; EXAMPLE 2 Preparation of <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> acetate (ester) STR7 Acetic anhydride (25 g) and pyridine (10 drops) is added to <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> (9 g, 0.1 mol). The reaction mixture is stirred overnight at room temperature, concentrated in vacuo and chased with xylene to give the title product as an oil (11.9 g, 0.9 mol) which is identified by 1 H-NMR spectral analysis. Following the above procedure, but substituting the appropriate N-(hydroxymethyl) compound for <strong>[625-51-4]N-(hydroxymethyl)acetamide</strong> yields the following compounds: N-(hydroxymethyl)benzamide acetate (ester); N-(hydroxymethyl)-2-thiophenecarboxamide acetate (ester); N-(hydroxymethyl)-2,2-dimethylpropionamide acetate (ester); 2,2,2-trifluoro-<strong>[625-51-4]N-(hydroxymethyl)-acetamide</strong> acetate (ester); N-(hydroxymethyl)-3-furamide acetate (ester); or N-(hydroxymethyl)-p-chlorobenzamide acetate (ester).
 

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