Trichlorosilane → Phenyltrichlorosilane

反応式

[C:1]1([Si:7](C)([CH3:9])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:11][SiH:12]([Cl:14])[Cl:13]>>[C:1]1([Si:12]([Cl:14])([Cl:13])[Cl:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:1][SiH:7]([CH3:9])[CH3:8]

参加物

反応物 2

HCID 24811Trichlorosilane

HCID 69849Phenyltrimethylsilane

生成物 2

HCID 7372Phenyltrichlorosilane

HCID 70435Trimethylsilane

実験手順

Eaborn et al., J. Organometal. Chem. 4:489 (1965). describes a process where phenyltrimethylsilane and trichlorosilane are reacted at 500° C. in the gas phase to give phenyltrichlorosilane and trimethylsilane.

後処理

customare reacted at 500° C. in the gas phase

出典と根拠

ORDレコード: ord-b3afc3e1e36a4748becb33e3cd128dab
出典データセット: uspto-grants-1992_06
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US05126471

反応ノート

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