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CAS No. : | 7298-67-1 | MDL No. : | MFCD00100490 |
Formula : | C10H11NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | DIQSYMRVTOVKQT-UHFFFAOYSA-N |
M.W : | 193.20 | Pubchem ID : | 81720 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
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* 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 |
---|---|---|
94% | for 6 h; Heating / reflux | 5-Acetamido-2-hydroxyacetophenone was hydrolyzed in 2N hydrochloric solution by refluxing for 6 hours, yielding 94percent of 5-amino-2-hydroxyacetophenone. |
94% | for 6 h; Heating / reflux | 5. p-Anisidine is acylated at the amino center with acetic anhydride in di- chloromethane and the acylated product was obtained in 91 percent yield . Then, Friedel Craft's acylation was carried out to get the hydroxyacetophenone derivative with acetyl chloride in the presence of anhydrous aluminium chloride in DCM. The intermediate was isolated in 70percent yield. δ-Acetamido^-hydroxyacetophenone was hydrolyzed in 2N hydrochloric solution by refluxing for 6 h, yielding 94percent of δ-amino^-hydroxyacetophenone. |
84% | for 0.666667 h; Heating / reflux | A suspension of [N- (3-ACETYL-4-HYDROXY-PHENYL)-] acetamide (1.029 g, 5.3 mmol) in [15percent] HC1 (1.5 ml, 6.2 mmol, 1.2 equ) was heated to reflux for 40 minutes, then cooled and neutralised with 10percent aqueous ammonia. The precipitated solid was collected by filtration as 1- (5-amino-2-hydroxy- phenyl) -ethanone (0.677 g, 84percent) a green solid. [APOS;H] nmr (400 MHz, CDC13) 2.58 (s, 3H) 3.47 (brs, 2H) 6.83 (d, [1H,] 8.8 Hz) 6.91 (dd, 1H, 2.8+8. 8 Hz) 7.02 (d, 1H, 2.8 Hz). 13C nmr (100 MHz, [CDC13)] 27.12 [(CH3)] 115.71 (CH) 119.40 (CH) 119.87 [(Q)] 125.737 (CH) 138.40 (Q) 156.03 (Q) 204.48 [(Q). EI+ 151.] 1 [(100percent, M+) C8HGNO2] Calc. 151.0633 Found 151.0632. |
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