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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262857Generated: October 26, 2026

Iodine → 1-Iodo-4-trimethylsiloxy-trans-1-octene

https://huagongshe.com/reaction/262857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTrimethylamine oxideHCID 1145—
ReactantSodium HydroxideHCID 14798—
ReactantBis(1,2-dimethylpropyl)boraneHCID 192733—
ReactantTrimethyl[(oct-1-yn-4-yl)oxy]silaneHCID 12786181—
SolventTetrahydrofuranHCID 8028—
Product1-Iodo-4-trimethylsiloxy-trans-1-octeneHCID 12851277—

Reaction Steps

To a stirred solution of 0.20 moles of freshely prepared bis-(3-methyl-2-butyl)borane in 300 ml of tetrahydrofuran at 0°-5° C. is added dropwise a solution of 19.8 g of 4-trimethylsiloxy-1-octyne in 30 ml of tetrahydrofuran. The resulting mixture is stirred at ambient temperature for several hours, cooled in an ice bath, and treated with 53 g of trimethylamine oxide. The mixture is stirred several hours at 25°-40° C. and then poured into 2 liters of 15% sodium hydroxide. The resulting mixture is treated immediately with a solution of 140 g of iodine in 300 ml of tetrahydrofuran. After 0.5 hour the organic phase is-separated and the aqueous phase is extracted with ether. The combined organic layers are washed with water, sodium thiosulfate solution, and brine; dried over magnesium sulfate; and concentrated to give an oil, pmr spectrum (CDCl3): 6.2 (d, ICH=) and 6.7 (quintuplet, =CH--).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154959
Source datasetuspto-grants-1979_05
ORD IDord-33c150c393af43c986c4750a66d9e557
Source noteuspto-grants-1979_05