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Benzyltriethylammonium chloride (BTEAC)

  • Product Name: Benzyltriethylammonium chloride (BTEAC)
  • CAS: 56-37-1
  • Purity:
  • Appearance: white to light yellow crystallize powder

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What is the Benzyltriethylammonium chloride ?

Benzyltriethylammonium chloride is white to light yellow crystallize powder, while it's Molecular Formula is C13H22ClN. Benzyltriethylammonium chloride is used as a catalyst in the preparation of 2-phenylbutyronitrile from phenyl acetonitrile. It is involved in the Knoevenagel condensation of carbonyl compounds with active methylene compounds to give olefinic products. It acts as a phase transfer catalyst used in the alkylation reaction. It reacts with 1H-Pyridine-2-thione to get 2-Benzylsulfanyl-pyridine.

What is the CAS number for Benzyltriethylammonium chloride ?

The CAS number of Benzyltriethylammonium chloride is 56-37-1.

More information of Benzyltriethylammonium chloride 56-37-1 are:

Synonyms

Ammonium,benzyltriethyl-, chloride (8CI);Benzenemethanaminium, N,N,N-triethyl-,chloride (9CI);Benzyltriethylammonium chloride (6CI);BAC-TE;N,N,N-Triethyl-N-benzylammonium chloride;TEBA;TEBAC;Triethylbenzylammoniumchloride;Benzenemethanaminium, N,N,N-triethyl-, chloride;

CAS Number

56-37-1

Molecular Formula

C13H22ClN

Molecular Weight

227.777

Density

1.08 g/mL at 25 °C

Melting Point

239 °C (dec.)(lit.)

Boiling Point

366.11°C (rough estimate)

Flash Point

> 100 °C

HS CODE

2923.90

PSA

0.00000

LogP

0.06710

What is Benzyltriethylammonium chloride (56-37-1) used for?

Benzyltriethylammonium chloride (TEBAC) is a phase transfer catalyst (PTC) used in organic synthesis to facilitate reactions between immiscible phases, such as aqueous and organic layers. It has been employed in the synthesis of 6-methoxytryptamine, where it enhances the alkylation step by improving the reactivity of the reactants in a biphasic system. Additionally, it serves as a chloride source in radical-mediated chlorodecarboxylation reactions, influencing product distributions based on its concentration. Its role as a PTC also extends to the synthesis of heterocyclic compounds like N-thioamido-β-lactams, where it increases reaction efficiency and yield under mild conditions.

InChI:InChI=1/C13H22N.ClH/c1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;/h7-11H,4-6,12H2,1-3H3;1H/q+1;/p-1

Articles related to Benzyltriethylammonium chloride:

Article

Source

Activation of C-Cl Bonds in Chloroalkanes by Nickel Oxide Nanoparticles: Formation of Tetrasubstituted Ammonium Salts from Tertiary Amines

Park, Kang Hyun,Jung, Il Gu,Chung, Young Keun,Han, Jin Wook

, p. 411 - 416 (2007)

Thermal stability of quaternary ammonium hexafluorophosphates and halides

Zhuravlev,Nikol'skii,Voronchikhina

, p. 824 - 830 (2014/02/14)

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