Alternatived Products of [ 35356-70-8 ]
Product Details of [ 35356-70-8 ]
CAS No. : | 35356-70-8 |
MDL No. : | MFCD00013394 |
Formula : |
C6H9NO3
|
Boiling Point : |
- |
Linear Structure Formula : | CH3C(O)NHC(CH2)C(O)OCH3 |
InChI Key : | SMWNFFKPVLVOQQ-UHFFFAOYSA-N |
M.W : |
143.14
|
Pubchem ID : | 98644 |
Synonyms : |
|
Chemical Name : | Methyl 2-acetamidoacrylate |
Application In Synthesis of [ 35356-70-8 ]
* 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 [ 35356-70-8 ]
- 1
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[ 35356-70-8 ]
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[ 452-79-9 ]
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[ 581101-43-1 ]
- 2
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[ 35356-70-8 ]
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[ 262373-15-9 ]
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[ 1006707-80-7 ]
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[ 1006707-81-8 ]
- 3
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[ 641144-16-3 ]
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[ 35356-70-8 ]
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[ 1227732-28-6 ]
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[ 121848-75-7 ]
- 4
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[ 641144-16-3 ]
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[ 35356-70-8 ]
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[ 1227732-29-7 ]
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[ 121848-75-7 ]
- 5
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[ 35356-70-8 ]
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[ 181765-85-5 ]
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[ 1426383-93-8 ]
Yield | Reaction Conditions | Operation in experiment |
69% |
With tetrabutylammomium bromide; palladium diacetate; sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 85 - 90℃; for 20h;Inert atmosphere; |
Methyl 4-chloro-2-iodobenzoate (284 mg, 0.96 mmol) is dissolved in DMF (2 mL) then methyl 2-acetamidoacrylate (205 mg, 1 .44 mmol), tetrabutylammonium bromide (308 mg, 0.96 mmol), NaHCO3 (201 mg, 2.39 mmol) and palladium (II) acetate (1 1 mg, 0.05 mmol) are added. The reaction mixture is heated at 85-90 C for 20 h under argon atmosphere. At the begining the reaction mixture is red, but after 10 min turned to dark red. After 20 h the reaction mixture is cooled to rt and 25 mL of water are added. The heterogenous solution is filtered, washed with small portions of water and dried to give the title compound (157 mg, 69%) as a brown solid. 1H-NMR (200 MHz, DMSO-de), delta: 3.86 (s, 3H); 7.41 (s, 1 H); 7.64 (d, 8.8 Hz, 1 H); 8.05 (s, 1 H); 8.20 (d, 8.8 Hz, 1 H). LC-MS: 238 [M+H]. |