• Product Nametert-Butylchlorodiphenylsilane
  • CasNo. 58479-61-1
  • MFC16H19ClSi
  • MW274.865
  • Purity
  • AppearanceColorless-light yellow to brown liquid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 58479-61-1

MF: C16H19ClSi

Appearance: Colorless-light yellow to brown liquid

Chinese Manufacturer Supply 99% Pure 58479-61-1 with Fast Shipping

  • Molecular Formula:C16H19ClSi
  • Molecular Weight:274.865
  • Appearance/Colour:Colorless-light yellow to brown liquid 
  • Vapor Pressure:0.000249mmHg at 25°C 
  • Refractive Index:n20/D 1.568(lit.)  
  • Boiling Point:334.4 °C at 760 mmHg 
  • Flash Point:143.3 °C 
  • PSA:0.00000 
  • Density:1.04 g/cm3 
  • LogP:3.78520 

tert-Butylchlorodiphenylsilane(Cas 58479-61-1) Usage

Preparation

a dry 1 L, three-necked round bottomed flask is equipped with a magnetic stirring bar, a 500mL equalizing dropping funnel fitted with a rubber septum, a reflux condenser, and nitrogen inlet tube. The flask is flushed with nitrogen, then charged with 127 g (0.5 mol) of diphenyldichlorosilane in 300mL of redistilled pentane. A solution of tbutyllithium in pentane (500 mL, 0.55 mol), is transferred under nitrogen pressure to the dropping funnel using a stainless steel, double-tip transfer needle. This solution is slowly added to the contents of the flask and when the addition is complete, the mixture is refluxed 30 h under nitrogen with stirring. The suspension is allowed to cool to rt, the precipitated lithium chloride is rapidly filtered through a pad of Celite, and the latter is washed with 200mL of pentane. The solvent is removed by evaporation, and the colorless residue is distilled through a short (10 cm), Vigreux column, to give 125–132 g of the colorless title compound.

Purification Methods

Purify it by repeated fractional distillaton. It is soluble in DMF and pentane [Hanessian & Lavalee Can J Chem 53 2975 1975, Robl et al. J Med Chem 34 2804 1991]. [Beilstein 4 IV 4076 for tert-butylchlorodimethylsilane.]

Physical properties

colorless liquid, bp 93–95°C/0.015 mmHg; n20 D 1.5680; d 1.057 g cm?3.

InChI:InChI=1/C16H19ClSi/c1-16(2,3)18(17,14-10-6-4-7-11-14)15-12-8-5-9-13-15/h4-13H,1-3H3

58479-61-1 Relevant articles

Synthesis of (±)-diplodialide B and A

Shenvi,Gerlach

, p. 2426 - 2433 (1980)

-

Functional Group Variation in tert-Butyldiphenylsilanes (TBDPS): Syntheses, Reactivities, and Effects on the Intermolecular Interaction Pattern in the Molecular Crystalline State

Bauer, Jonathan O.,Espinosa-Jalapa, Noel Angel,Fontana, Nicolò,G?tz, Tobias,Falk, Alexander

, p. 2636 - 2642 (2021/06/17)

We present the preparation of tert-butyl...

METHOD FOR PRODUCING HALOSILANE COMPOUND HAVING TERTIARY HYDROCARBON GROUP

-

Paragraph 0028-0031; 0033-0037, (2019/12/13)

PROBLEM TO BE SOLVED: To provide a metho...

Neutral-Eosin-Y-Photocatalyzed Silane Chlorination Using Dichloromethane

Fan, Xuanzi,Xiao, Pin,Jiao, Zeqing,Yang, Tingting,Dai, Xiaojuan,Xu, Wengang,Tan, Jin Da,Cui, Ganglong,Su, Hongmei,Fang, Weihai,Wu, Jie

supporting information, p. 12580 - 12584 (2019/08/16)

Chlorosilanes are versatile reagents in ...

Iron-catalyzed chlorination of silanes

Savela, Risto,Zawartka, Wojciech,Leino, Reko

experimental part, p. 3199 - 3206 (2012/06/04)

A simple and highly efficient iron-catal...

58479-61-1 Process route

tertiary butyl chloride
507-20-0

tertiary butyl chloride

diphenylsilyl dichloride
80-10-4

diphenylsilyl dichloride

tert-butylchlorodiphenylsilane
58479-61-1

tert-butylchlorodiphenylsilane

Conditions
Conditions Yield
tertiary butyl chloride; With magnesium; In tetrahydrofuran; at 60 ℃; for 2h;
With lithium chloride; copper(I) bromide; In tetrahydrofuran; at 20 ℃; for 1h;
diphenylsilyl dichloride; In tetrahydrofuran; at 50 ℃; for 6h; Reagent/catalyst; Temperature;
87%
With copper(l) cyanide; magnesium; In tetrahydrofuran; for 5h; Heating;
80%
With magnesium; In tetrahydrofuran; hexane;
75%
diphenylsilyl dichloride
80-10-4

diphenylsilyl dichloride

tert-butylchlorodiphenylsilane
58479-61-1

tert-butylchlorodiphenylsilane

Conditions
Conditions Yield
copper (II) acetylacetonate;
85%

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