CasNo: 78-09-1
Molecular Formula: C9H20O4
Appearance: clear colorless liquid
Chemical Properties |
clear colorless liquid |
Uses |
Tetraethyl Orthocarbonate is used in the synthesis of chemokine receptor-5 inhibitors against HIV-1, benzobisoxazoles and in the preparation of organic semiconductors. It is also employed in the synthesis of 2,7-dimethylene-1,4,6,9-tetraoxaspiro[4,4]nonane and in the synthesis of cross linked poly(orthocarbonate)s used as organic solvent absorbent. |
Purification Methods |
Likely impurities are hydrolysis products. Shake the orthocarbonate with brine (saturated NaCl, dilute with a little Et2O if amount of material is small) and dry (MgSO4). The organic layer is filtered off and evaporated, and the residue is distilled through a helices packed fractionating column with a total reflux partial take-off head. All distillations can be done at atmospheric pressure in an inert atmosphere (e.g. N2). [Roberts & McMahon Org Synth Coll Vol IV 457 1963, Connolly & Dyson J Chem Soc 828 1937, Tieckelmann & Post J Org Chem 13 266 1948, for review see Kantlehner et al. Justus Liebigs Ann Chem 507 207 1982, Beilstein 3 IV 6.] |
InChI:InChI=1/C9H20O4/c1-5-10-9(11-6-2,12-7-3)13-8-4/h5-8H2,1-4H3
The invention relates to the field of re...
The invention relates to a synthesis met...
An unexpected modulation of the chemosel...
A process for producing crystals of 2-et...
triethoxyacetonitrile
benzylamine
orthocarbonic acid tetraethyl ester
Diethyl(benzylimido)carbonat
1,3-Dibenzyl-2-ethylisoharnstoff
Conditions | Yield |
---|---|
at 120 ℃;
|
14% 45% |
at 120 ℃;
Heating;
|
45% 14% |
ethanol
chloropicrin
orthocarbonic acid tetraethyl ester
Conditions | Yield |
---|---|
With
sodium ethanolate;
at 65 - 70 ℃;
for 3h;
Temperature;
Large scale;
|
91% |
With
sodium;
Darst.;
|
tetrachloromethane
sodium ethanolate
diethyl ether
carbon tetrabromide
nonanone-5
pentan-3-one
2,4-dimethylpentan-3-one
4-heptanone
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