(2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane

Base Information

• Chemical Name: (2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane
• CAS No.: 91425-17-1
• Molecular Formula: C21H39PSi
• Molecular Weight: 350.6
• DSSTox Substance ID: DTXSID40587128
• Wikidata: Q82479435
• Mol file: 91425-17-1.mol

Synonyms:(2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane;91425-17-1;DTXSID40587128

Chemical Property of (2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane

Chemical Property:

• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 5
• Exact Mass: 350.25586478
• Heavy Atom Count: 23
• Complexity: 362

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)P[Si](C)(C)C)C(C)(C)C

Technology Process of (2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane

There total 1 articles about (2,4,6-Tri-tert-butylphenyl)(trimethylsilyl)phosphane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

chloro-trimethyl-silane (75-77-4) + (2,4,6-tri-tert-butylphenyl)phosphine (83115-12-2) → (2,4,6-tri-tert-butylphenyl)(trimethylsilyl)phosphane (91425-17-1)

Guidance literature:

With n-butyllithium; Yield given. Multistep reaction; 1.) hexane, THF, -78 deg C, 1 h, 2.) -78 deg C, 0.5 h;

Reference yield: 82.0%

P,P-dichloroferrocenylphosphine (1291-31-2) + (2,4,6-tri-tert-butylphenyl)(trimethylsilyl)phosphane (91425-17-1) → (E)-1-ferrocenyl-2-(2,4,6-tri-tert-butylphenyl)diphosphene (173602-83-0)

Guidance literature:

With n-butyllithium; In diethyl ether; hexane; byproducts: LiCl; Ar-atmosphere; stirring (-78°C, 30 min, room temp., 1.5 h), Fe-complex soln. (Et2O) addn. (-78°C); evapn. (vac., room temp.), extg. (pentane), filtering, evapn. (vac.);

DOI:10.1021/om950384f

Reference yield: 57.0%

dichloro(pentamethylcyclopentadienyl)arsine (79055-04-2) + (2,4,6-tri-tert-butylphenyl)(trimethylsilyl)phosphane (91425-17-1) → P-(2,4,6-Tri-t-butylphenyl)-As-(pentamethylcyclopentadienyl)phosphaarsen (111398-02-8,111662-44-3)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; hexane; from -78 degC to room t.;

DOI:10.1016/0022-328X(87)80131-6

upstream raw materials:

chloro-trimethyl-silane

(2,4,6-tri-tert-butylphenyl)phosphine

Downstream raw materials:

3-(2,4,6-tri-tert-butylphenylphosphinylidene)quadricyclane

C₂₂H₄₀ClNP₂

P-(2,4,6-Tri-t-butylphenyl)-P'-(pentamethylcyclopentadienyl)diphosphen

(((CH₃)3C)3C₆H₂P)(((CH₃)3C)3C₆H₂PH)COSi(CH₃)3