Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726828Generated: October 25, 2026

Iodine → [(S)-2-methylbutyl]phenyldichlorosilane

https://huagongshe.com/reaction/726828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPhenyltrichlorosilaneHCID 7372—
ReactantMagnesiumHCID 5462224—
Reactant1-Bromo-2-methylbutane, (+)-HCID 5464167—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product[(S)-2-methylbutyl]phenyldichlorosilaneHCID 67606162—

Reaction Steps

Anhydrous tetrahydrofuran (125 mL) was put into a reactor with magnesium (5.7 g, 0.24 mol) and molecular sieves 4A which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. (S)-(+)-1-bromo-2-methylbutane (30 g, 0.20 mol) was added dropwise to the slowly stirred mixture so that the reaction mixture was gradually refluxed. After the reaction was complete, the obtained Grignard reagent was transferred to a dropping funnel. The Grignard reagent was added dropwise to a solution being stirred containing phenyltrichlorosilane (50 g, 0.24 mol) in anhydrous tetrahydrofuran (50 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 40° C.-50° C. The reaction mixture was then stirred overnight at room temperature. Hexane (500 mL) was added to the reaction mixture, and the resulting mixture was filtered under pressure, followed by fractional distillation of the filtrate to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710301
Source datasetuspto-grants-1998_01
ORD IDord-68b0b1270932435b9b009a92f1bad50d
Source noteuspto-grants-1998_01