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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66402Generated: October 25, 2026

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

https://huagongshe.com/reaction/66402

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 0.020 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 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 (CDCl 3): 6.2 (d, ICH=) and 6.7 (quintuplet, =C-).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04131737
Source datasetuspto-grants-1978_12
ORD IDord-ee8814a93a8044e3904426eff2a6053d
Source noteuspto-grants-1978_12