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Butyldi-1-adamantylphosphine

Butyldi-1-adamantylphosphine

CAS: 321921-71-5

Molecular Formula: C24H39P

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Butyldi-1-adamantylphosphine - Names and Identifiers

Name Butyldi-1-adamantylphosphine
Synonyms CATACXIUM A
cataCXium(R) A
Butyldi-1-adamantylphosphine
BUTYLDI-1-ADAMANTYLPHOSPHINE
nbutyl-di(1-adamantyl)phosphine
Diadamantan-1-yl(butyl)phosphine
Di(1-adamantyl)-n-butylphosphine
Di(adamantan-1-yl)(butyl)phosphine
BUTYLDI-1-ADAMANTYLPHOSPHINE [CATACXIUM A]
CAS 321921-71-5
EINECS 691-708-4
InChI InChI=1/C24H39P/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24/h17-22H,2-16H2,1H3
InChIKey HTJWUNNIRKDDIV-UHFFFAOYSA-N

Butyldi-1-adamantylphosphine - Physico-chemical Properties

Molecular FormulaC24H39P
Molar Mass358.54
Melting Point100°C
Boling Point449.6±12.0 °C(Predicted)
Flash Point239°C
Vapor Presure7.51E-08mmHg at 25°C
AppearanceCrystalline powder
Colorwhite to yellow
BRN8726448
Storage ConditionInert atmosphere,Room Temperature
Sensitiveair sensitive
MDLMFCD05861606

Butyldi-1-adamantylphosphine - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany3
HS Code29310095

Butyldi-1-adamantylphosphine - Reference Information

Use n-butyldi (1-adamantyl) phosphine is a catalyst. n-butyl di (1-adamantyl) phosphine is an electron-rich phosphine ligand used in palladium-catalyzed cross-coupling reactions such as Heck and Suzuki coupling reactions.
Application n-butyl di (1-adamantyl) phosphine is a novel phosphine ligand, which can be made of di (1-adamantyl) phosphine and di-n-butyl ether in one step to prepare hi is obtained. Although palladium (0)/nickel (0) compounds are known as present reaction catalysts, palladium and nickel catalysts for activating and refining halogenated aromatic compounds with
are palladium (II) and/or nickel (II) and palladium (0) and/or nickel (0) complexes.
preparation 4.6g(15mmol) di (1-adamantyl) phosphine was placed in 50ml di-n-butyl ether and 20ml of 2.5Mn-BuLi(50mmol) toluene solution was added. The solution was refluxed for 1 hour and cooled, and 2.8g(30mmol) of 1-butyl chloride was added dropwise. The mixture was refluxed for 30 minutes, cooled and washed with a saturated ammonium chloride solution (3x), the organic phase was separated and dried on sodium sulfate and the solvent was distilled off under reduced pressure. The product was purified by spherical tube distillation under high vacuum. Yield: 4.6g(13mmol,85%) n-butyl di (1-adamantyl) phosphine.
Last Update:2024-04-10 22:29:15
Butyldi-1-adamantylphosphine
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