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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083513Generated: October 28, 2026

Iodine → HCID 12884304, compound

https://huagongshe.com/reaction/2083513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTrimethylamine oxideHCID 1145—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium HydroxideHCID 14798—
ReactantBis(1,2-dimethylpropyl)boraneHCID 192733—
ReactantSodium borohydrideHCID 4311764—
ReactantSilane, trimethyl[[1-methyl-1-(2-propynyl)pentyl]oxy]-HCID 10856810—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 12884304HCID 12884304—

Reaction Steps

To a stirred solution of 400 ml of 0.5 M bis-(3-methyl-2-butyl)borane in glyme, prepared from sodium borohydride, 2-methyl-2-butene, and boronitrifluoride etherate as in Example 107, is added 63.7 g (0.30 moles) of 4-methyl-4-trimethylsilyloxy-1-octyne (Example 125) at -10° C. The solution is stirred at ambient temperature for 2.5 hours, cooled to -10° C, and treated during 30 minutes with 158 g (2.1 moles) of solid trimethylamine oxide with cooling. The mixture is stirred at ambient temperature for 2 hours and then poured into a stirred, ice-cold solution of 15% aqueous sodium hydroxide; the stirred mixture is treated immediately with a solution of 426 g (1.68 moles) of iodine in 1100 ml of tetrahydrofuran. After 4 hours the mixture is extracted with ether. The extract is washed successively with water, aqueous sodium thiosulfate, and brine and dried over magnesium sulfate. The extract is concentrated, and the residue is subjected to chromatography on silica gel with hexane to provide an oil, p.m.r. (CDCl3): δ 1.18 (singlet, 4-CH3 group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085272
Source datasetuspto-grants-1978_04
ORD IDord-b2a2a9f724d54a62bb9dc541ef51bd79
Source noteuspto-grants-1978_04