Phenylsilane

Author:

Yang Junyu,Ali Siraj,Radosevich Alexander T.

Abstract

image [694‐53‐1] C 6 H 5 SiH 3 (MW 108.22) InChI =  1S/C6H8Si/c7‐6‐4‐2‐1‐3‐5‐6/h1‐5H,7H3 InChiKey =  PARWUHTVGZSQPD‐UHFFFAOYSA‐N (reagent used as reductant in catalysis) Physical Data : bp 120 °C (750 torr) 1 ; density = 0.8775 g mL −2 . Solubility : soluble in most organic solvents; releases flammable gas upon contact with water. Form Supplied : clear, colorless oil, commercially available. Analysis of Reagent Purity : purity is analyzed by 1 H NMR (500 MHz, CD 2 Cl 2 ): δ 4.19 (s, 3 H ), 7.36–7.41 (m, 3 H ), 7.37 (d, J  = 7.6 Hz, 2 H ); 13 C{1 H } NMR (126 MHz, CD 2 Cl 2 ): δ 128.7 (s, 2C), 130.4 (s), 136.2 (s), 136.4 (s, 2C), and 29 Si DEPT NMR (99 MHz, CD 2 Cl 2 ) δ −59.8. 2 Preparative Method : reduction of phenyltrichlorosilane or phenyltriethoxysilane with lithium aluminum hydride in ether. 1,3 Purification : distillation under nitrogen at room temperature and atmospheric pressure. 4 Handling, Storage, and Precautions : flammable. Stable at room temperature in closed containers. Phenylsilane is capable of releasing hydrogen gas upon storage, particularly in the presence of acids, bases, or fluoride‐releasing salts. 5 Precautions should be taken to vent possible hydrogen buildup when opening vessels in which phenylsilane is stored.

Publisher

Wiley

Reference92 articles.

1. The Addition of Silicon Hydrides to Olefinic Double Bonds. Part I. The Use of Phenylsilane, Diphenylsilane, Phenylmethylsilane, Amylsilane and Tribromosilane

2. Custom Hydrosilane Synthesis Based on Monosilane

3. The Cleavage of sym-Diphenyldisiloxane by Organometallic Compounds

4. Phenylsilane 97%; CAS RN: 694‐53‐1; 335150; rev. 6.4; Sigma Aldrich Co. LLC.: St. Louis MO August 2 2023.https://www.sigmaaldrich.com/US/en/sds/aldrich/335150(accessed Nov. 01 2023).

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