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CAS No. : | 27829-72-7 | MDL No. : | MFCD00036541 |
Formula : | C8H14O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | SJRXWMQZUAOMRJ-VOTSOKGWSA-N |
M.W : | 142.20 | Pubchem ID : | 5364778 |
Synonyms : |
|
Chemical Name : | Ethyl (E)-hex-2-enoate |
Signal Word: | Danger | Class: | 3 |
Precautionary Statements: | P210-P280-P370+P378-P403+P235-P501 | UN#: | 3272 |
Hazard Statements: | H225 | Packing Group: | Ⅲ |
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 |
---|---|---|
99.4% | With 1,8-diazabicyclo[5.4.0]undec-7-ene; at 0 - 20℃; for 3h; | 1.a. Synthesis of 3-nitromethyl-hexanoic acid ethyl ester (B)(A) (B)To a stirred solution of hex-2-enoic acid ethyl ester (A) (45Og, 3.164mol,leq) in nitromethane (858ml, 15.822 mol, 5 eq) cooled at O0C, is added dropwise, under nitrogen,481.8g (3.164 mol, leq.) of 1.8-diazabicyclo[5.4.0]undec-7-ene (DBU). The reaction mixture is allowed to react at room temperature for 3h and is quenched with a 6M aqueous hydrogen chloride solution to obtain pH = 4. The solution is extracted with diethyl ether (500ml + 2 x 300ml). The organic layers are dried with MgSpsi4, filtered and concentrated to obtain an oil residue (672.13g, HPLC purity = 78.9percent) which is purified by liquid EPO <DP n="24"/>chromatography eluting with dichloromethane. 639.4 Ig of 3-nitromethyl-hexanoic acid ethyl ester (B) are obtained (yield = 99.4percent).GC/MS : MH+ = 204 |
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