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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726831Generated: October 26, 2026

Iodine → n-Hexyl(2-ethylbutyl)dichlorosilane

https://huagongshe.com/reaction/726831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHexyltrichlorosilaneHCID 13571—
ReactantPentane, 3-(bromomethyl)-HCID 77432—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productn-Hexyl(2-ethylbutyl)dichlorosilaneHCID 19708028—

Reaction Steps

Anhydrous diethyl ether (100 mL) was put into a reactor with magnesium (5.0 g, 0.21 mol) which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. 2-Ethylbutylbromide (29.5 g, 0.18 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 n-hexyltrichlorosilane (38 g, 0.17 mol) in anhydrous tetrahydrofuran (100 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 60° C.-70° 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-f277a45bb71541ada25b3a3ae69ae793
Source noteuspto-grants-1998_01