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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848892Generated: October 25, 2026

Iodine → 1-Iodo-4-propadienyl-4-trimethylsilyloxy-trans-octene

https://huagongshe.com/reaction/848892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthanamine, N,N-diethyl-, N-oxideHCID 123168—
ReactantBis(1,2-dimethylpropyl)boraneHCID 192733—
Reactant4-Propadienyl-4-trimethylsilyloxy-1-octyneHCID 13039189—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-Iodo-4-propadienyl-4-trimethylsilyloxy-trans-octeneHCID 13039190—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 2.36 g. (10 mmol.) of 4-propadienyl-4-trimethylsilyloxy-1-octyne in 5 ml. of glyme is added a solution of 11 mmol. of bis-(3-methyl-2-butyl)borane in 15 ml. of glyme at 0° C. The mixture is stirred at 25° C. for 90 minutes, cooled to 0° C., and treated portionwise with 3.0 g. of triethylamine oxide. The stirred mixture is maintained at 25°-30° C. for 45 minutes, diluted with 20 ml. of tetrahydrofuran and poured into 100 ml. of ice-cold 15% sodium hydroxide solution, followed immediately with a solution of 8.0 g. of iodine in 20 ml. of tetrahydrofuran. The mixture is stirred at ambient temperature for 30 minutes and then extracted with ether. The extract is washed successively with water, sodium thiosulfate solution and brine; dried over magnesium sulfate; and filtered. The residue obtained after solvent evaporation is subjected to chromatography on silica gel with heptane solvent to afford the title compound as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297516
Source datasetuspto-grants-1981_10
ORD IDord-1de928bbe7f44bea988cead2cbf31c12
Source noteuspto-grants-1981_10