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CAS No. : | 6299-67-8 | MDL No. : | MFCD00180769 |
Formula : | C8H11NO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | HEZIOZBMPKPOER-UHFFFAOYSA-N |
M.W : | 153.18 | Pubchem ID : | 239603 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P501 | UN#: | |
Hazard Statements: | H302+H312+H332-H315-H319 | 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 |
---|---|---|
62% | With pyridine; In dichloromethane; at 0 - 20℃;Inert atmosphere; | General procedure: To a solution of 3,4-dimethoxyaniline (0.77 g, 5.0 mmol) in CH2Cl2 (8.0 mL) was added pyridine (4.0 mL, 50 mmol) and benzoyl chloride (0.70 g, 5.0 mmol) in CH2Cl2 (2.0 mL) at 0 C, and stirred at room temperature under argon. The reaction was monitored by TLC. The resulting mixture was quenched with 1M HCl, extracted with CH2Cl2 (3 x 20 mL). The combined organic layer was washed with brine, dried over MgSO4, and concentrated under vacuum. The crude compounds were purified with silica gel column chromatography (EtOAc : hexane = 1 : 2) and recrystallized from EtOAc/hexane to get the target anilide 1a (0.62 g, 48%). |
[ 860586-41-0 ]
2,3,4-Trimethoxyaniline hydrochloride
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