Intermediate of API

78-09-1

  • Product Name:Tetraethyl orthocarbonate (TEOC)
  • Molecular Formula:C9H20O4
  • Specifications:99%
  • Molecular Weight:192.255
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Product Details;

CasNo: 78-09-1

Molecular Formula: C9H20O4

Appearance: clear colorless liquid

Fast Delivery High Quality Tetraethyl orthocarbonate (TEOC) 78-09-1 In Bulk Supply

  • Molecular Formula:C9H20O4
  • Molecular Weight:192.255
  • Appearance/Colour:clear colorless liquid 
  • Vapor Pressure:3.24mmHg at 25°C 
  • Melting Point:222 °C 
  • Refractive Index:n20/D 1.392(lit.)  
  • Boiling Point:159.5 °C at 760 mmHg 
  • Flash Point:52.8 °C 
  • PSA:36.92000 
  • Density:0.948 g/cm3 
  • LogP:1.74370 

Tetraethyl orthocarbonate(Cas 78-09-1) Usage

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

78-09-1 Relevant articles

Method for efficiently rectifying and producing tetraethyl orthocarbonate

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Paragraph 0023-0028; 0029-0034; 0035-0040; 0041-0046, (2018/04/02)

The invention relates to the field of re...

A method for synthesizing original ester carbonate (by machine translation)

-

Paragraph 0023; 0024, (2020/02/07)

The invention relates to a synthesis met...

Mechanistic study of the ring-size modulation in Michael-Dieckmann type reactions of 2-acylaminoacrylates with ketene diethyl acetal

Avenoza, Alberto,Busto, Jesus H.,Canal, Noelia,Garcia, Jose I.,Jimenez-Oses, Gonzalo,Peregrina, Jesus M.,Perez-Fernandez, Marta

, p. 224 - 229 (2008/02/02)

An unexpected modulation of the chemosel...

CRYSTAL AND PROCESS FOR PRODUCING THE SAME

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Page 18, (2010/02/06)

A process for producing crystals of 2-et...

78-09-1 Process route

triethoxyacetonitrile
68714-37-4

triethoxyacetonitrile

benzylamine
100-46-9

benzylamine

orthocarbonic acid tetraethyl ester
78-09-1

orthocarbonic acid tetraethyl ester

Diethyl(benzylimido)carbonat
6263-03-2

Diethyl(benzylimido)carbonat

1,3-Dibenzyl-2-ethylisoharnstoff
81759-29-7

1,3-Dibenzyl-2-ethylisoharnstoff

Conditions
Conditions Yield
at 120 ℃;
14%
45%
at 120 ℃; Heating;
45%
14%
ethanol
64-17-5

ethanol

chloropicrin
76-06-2

chloropicrin

orthocarbonic acid tetraethyl ester
78-09-1

orthocarbonic acid tetraethyl ester

Conditions
Conditions Yield
With sodium ethanolate; at 65 - 70 ℃; for 3h; Temperature; Large scale;
91%
With sodium; Darst.;

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