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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220175Generated: October 29, 2026

Sodium Iodide → HCID 67530272, compound

https://huagongshe.com/reaction/2220175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHCID 67530784HCID 67530784—
SolventWaterHCID 962—
ProductHCID 67530272HCID 67530272—

Reaction Steps

This compound was prepared in a manner analogous to that of Step E of Example 2, by 1) the reaction of 1.0 gram (0.006 mole) of 7-methylchroman-4-one (ii) with 1.8 gram (0.018 mole) of trimethylsilyl cyanide, in the presence of 0.2 gram (catalyst) of aluminum chloride in 30 mL of toluene, affording an intermediate product, namely: 7-methyl-4-(1,1-dimethyl-1-silaethoxy)chromane-4-carbonitrile (cyano-silyl intermediate), then 2) the reaction of the 1-silaethoxy intermediate with 3 mL (0.024 mole) of trimethylsilyl chloride, 3.6 grams (0.024 mole) of sodium iodide, and 0.2 mL of water in 30 mL of acetonitirile, yielding 0.8 gram of subject compound. Contrary to Step E of Example 2, the hydrogenation step was not necessary to obtain the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417057B2
Source datasetuspto-grants-2008_08
ORD IDord-4b37dc3ba7584cb8bc35d436beef0d82
Source noteuspto-grants-2008_08