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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848859Generated: October 29, 2026

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

https://huagongshe.com/reaction/848859

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 freshly 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 gas 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 numberUS04297516
Source datasetuspto-grants-1981_10
ORD IDord-8903d8fd51b64e88a44113fff22cadef
Source noteuspto-grants-1981_10