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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290396Generated: October 27, 2026

Trimethylsilyl iodide → Ethanethioic acid S-[tetrahydro-5-(iodomethyl)-3-thienyl]ester

https://huagongshe.com/reaction/1290396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 54092544HCID 54092544—
SolventChloroformHCID 6212—
ProductEthanethioic acid S-[tetrahydro-5-(iodomethyl)-3-thienyl]esterHCID 54241013—

Reaction Steps

A 0° C. mixture, under argon, of 0.44 g of product from Example 139 in 5 ml of dry chloroform is treated with 0.55 ml of trimethylsilyl iodide. The reaction is stirred, in the dark, for 2 hours. The reaction is quenched with 100 ml of saturated sodium sulfite, extracted with methylene chloride and the layers separated. The organic layer is dried, filtered and concentrated in vacuo. The residue is purified by chromatography (silica gel: 0 -100% methylene chloride/hexane) to give 0.31 g of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750735
Source datasetuspto-grants-1998_05
ORD IDord-de4b2ab3c9ff4044ae5dd833a440b9a6
Source noteuspto-grants-1998_05