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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413573Generated: November 1, 2026

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

https://huagongshe.com/reaction/1413573

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 grams 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 grams 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 grams of iodine in 300 ml of tetrahydrofuran. After about 0.5 hour the organic phase is separated; then 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 numberUS04250325
Source datasetuspto-grants-1981_02
ORD IDord-4680c3d001d241218968b52d7a2c9b63
Source noteuspto-grants-1981_02