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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethanamine, N,N-diethyl-, N-oxide | HCID 123168 | — |
| Reactant | Bis(1,2-dimethylpropyl)borane | HCID 192733 | — |
| Reactant | 4-Propadienyl-4-trimethylsilyloxy-1-octyne | HCID 13039189 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-Iodo-4-propadienyl-4-trimethylsilyloxy-trans-octene | HCID 13039190 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04297516 |
|---|
| Source dataset | uspto-grants-1981_10 |
|---|
| ORD ID | ord-1de928bbe7f44bea988cead2cbf31c12 |
|---|
| Source note | uspto-grants-1981_10 |
|---|