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CAS No. : | 52373-72-5 | MDL No. : | MFCD00066527 |
Formula : | C7H12O4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | DOWWCCDWPKGNGX-RXMQYKEDSA-N |
M.W : | 160.17 | Pubchem ID : | 853166 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H227-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
97% | Stage #1: With lithium hydroxide; water In tetrahydrofuran at 0℃; for 1.16667 h; Stage #2: With phosphoric acid In water |
Preparation 29:; (R)-2, 2-Dimethyl-1, 3-dioxolane-4-carboxylic acid; To a solution of methyl- (R)-2, 2-dimethyl-1, 3-dioxolane-4-carboxylate (1.8 grams, 11.24 mmol) in THF (20 mL) was added an aqueous solution (20 mL) of lithium hydroxide monohydrate (0.71 grams, 16.9 mmol) drop wise over a period of 10 minutes at 0 °C and stirring was continued for another 1 hour. The reaction mixture was diluted with 50 mL of water and extracted with ethyl acetate (50 mL), which was discarded. Further, the aqueous layer was acidified with 10 M phosphorous acid (H3PO4) and the pH was brought to 2. The aqueous layer was then extracted with ethyl acetate (50 mL x 4) and the combined organic layers were washed with water and brine and dried over sodium sulfate. Removal of volatiles left 1.6 grams (97percent) of the title acid, which was used directly for the next step. |
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