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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374268Generated: October 26, 2026

Iodine → HCID 86745717, compound

https://huagongshe.com/reaction/374268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantFarnesolHCID 445070—
ReactantTributyl(iodomethyl)stannaneHCID 10862926—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86745717HCID 86745717108.3%

Reaction Steps

A 1.15 g (10.0 mmol) of 35% KH in mineral oil was washed with three 5 mL portions of dry hexane and suspended in 15 mL of dry tetrahydrofuran (THF) under argon. A solution of 242 mg (0.95 mmol) of iodine in 10 mL of THF was added over 50 minutes and the reaction was allowed to stir for an additional 40 minutes at room temperature to give a white suspension. (E,E)-Farnesol (1.5 g, 6.75 mmol) in 10 mL of THF was added dropwise over 15 minutes, and after 75 minutes, a solution of 2.43 g (5.64 mmol) of tributyl(iodomethyl)tin was added rapidly in 6 mL of THF. The mixture was stirred for three hours and carefully quenched with methanol. Upon dilution with diethyl ether, the organic layer was washed with water and brine, dried (MgSO4) and evaporated to give 3.21 g of a pale yellow liquid. The crude material was chromatographed on 720 g of silica gel eluted with 0.5:99.5 diethyl ether: petroleum ether, and the impure fractions were further purified on 150 g of silica gel eluted with 0.33:99.67 diethyl ether:petroleum ether to provide a total of 2.09 g (71%) of pure title stannane as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166386
Source datasetuspto-grants-1992_11
ORD IDord-a87b08887cd74f6282136bf20e43b6eb
Source noteuspto-grants-1992_11