13716-10-4

  • Product NameDi-tert-butylchlorophosphane
  • Molecular FormulaC8H18ClP
  • Molecular Weight180.65
  • Purity99%
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Product Details

Quick Details

  • CasNo: 13716-10-4
  • Molecular Formula: C8H18ClP
  • Purity: 99%

High Purity Di-tert-butylchlorophosphane 13716-10-4 In Bulk Supply

  • Molecular Formula:C8H18ClP
  • Molecular Weight:180.658
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.71mmHg at 25°C 
  • Melting Point:2-3 °C 
  • Refractive Index:n20/D 1.482(lit.)  
  • Boiling Point:191.6 °C at 760 mmHg 
  • Flash Point:61.1 °C 
  • PSA:13.59000 
  • Density:0.951 g/mL at 25 °C(lit.) 
  • LogP:4.21910 

Di-tert-butylchlorophosphane(Cas 13716-10-4) Usage

Chemical Properties

Colorless to light yellow liqui

Uses

Di-tert-butylchlorophosphine is associated with palladium(II) acetate and used in Suzuki-Miyaura cross-couplings of arylboronic acids with aryl bromides and chlorides. It serves as a ligand and used in the preparation of mono- and bidentate phosphine ligands in metal complexes for catalytic chiral asymmetric hydrogenations. Further, it is used in asymmetric and transition metal coupling reactions. In addition to this, it plays an important role in the preparation of other phosphines in catalytic polymerization reactions.

Application

Bulky ligand used with Pd(OAc)2 in efficient Suzuki-Miyaura cross-couplings of arylboronic acids with aryl bromides and chlorides.

Precautions

Air and moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents and strong reducing agents.

InChI:InChI=1/C8H18ClP/c1-7(2,3)10(9)8(4,5)6/h1-6H3

13716-10-4 Relevant articles

Ga(N,P) Growth on Si and Decomposition Studies of the N-P Precursor Di- tert-butylaminophosphane (DTBAP)

Glowatzki, Johannes,H?nisch, Carsten Von,Hepp, Thilo,K?ster, Marcel,Ma?meyer, Oliver,Odofin, Ebunoluwa,Stolz, Wolfgang,Volz, Kerstin

, p. 1772 - 1781 (2020)

III/V semiconductors containing small am...

Novel sterically hindered ferrocenyl-phosphonium salt

Kadyrgulova, Liliya,Ermolaev, Vadim,Gilmanova, Leysan,Miluykov, Vasiliy

, p. 989 - 991 (2019)

New sterically hindered ferrocenyl conta...

Synthesis of ternary group 13/15 chain compounds

K?ster, Marcel,Kreher, Annikka,Von H?nisch, Carsten

, p. 7875 - 7878 (2018)

Herein we present the synthesis and char...

Ferrocene-containing sterically hindered phosphonium salts

Ermolaev, Vadim,Gerasimova, Tatiana,Kadyrgulova, Liliya,Shekurov, Ruslan,Dolengovski, Egor,Kononov, Aleksandr,Miluykov, Vasily,Sinyashin, Oleg,Katsyuba, Sergei,Budnikova, Yulia,Khrizanforov, Mikhail

, (2018/10/31)

The synthesis and physical properties of...

13716-10-4 Process route

tertiary butyl chloride
507-20-0

tertiary butyl chloride

di(tert-butyl)chlorophosphine
13716-10-4

di(tert-butyl)chlorophosphine

Conditions
Conditions Yield
tertiary butyl chloride; With magnesium; In diethyl ether; at 20 ℃; Inert atmosphere; Schlenk technique;
With phosphorus trichloride; In diethyl ether; at -40 ℃; Inert atmosphere; Schlenk technique;
50%
tertiary butyl chloride; With magnesium; In diethyl ether; at 20 ℃; Inert atmosphere; Schlenk technique;
With phosphorus trichloride; In diethyl ether; at -40 ℃; Inert atmosphere; Schlenk technique;
50%
Multistep reaction; (i) Mg, Et2O, (ii) PCl3;
 
di-tert-butylphosphine
819-19-2

di-tert-butylphosphine

di(tert-butyl)chlorophosphine
13716-10-4

di(tert-butyl)chlorophosphine

Conditions
Conditions Yield
With n-octyl trichloroacetate; at 70 - 84 ℃; for 0.666667h; Product distribution / selectivity;
78.2%
With tetrachloromethane; at 20 ℃; for 48h; Yield given; also at 100 deg C, 30 min.;
 

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