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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252397Generated: October 30, 2026

Tetrahydrofuran → HCID 86618879, compound

https://huagongshe.com/reaction/252397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86618880HCID 86618880—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86618879HCID 86618879—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.29 g of trimethylsulphoxonium iodide and 0.66 g of potassium tert-butoxide are stirred under high vacuum overnight, admixed with 8 ml of tetrahydrofuran and subsequently cooled to 0° C. A solution of 1.01 g of tert-butyl {1-formyl-3-[3-(3-methoxypropyl)-1-methyl-1H-indol-5-ylmethyl]-4-methylpentyl}carbamate in 8 ml of dimethyl sulphoxide is added dropwise. On completion of reaction (TLC monitoring), the reaction mixture is partitioned between water and tert-butyl methyl ether, and the aqueous phase is extracted once more with tert-butyl methyl ether (2×). The combined organic phases are washed successively with water (3×) and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is identified on the basis of the Rf value from the residue by means of flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868036B2
Source datasetuspto-grants-2011_01
ORD IDord-4864716cc5ce432f9ef8a496cee439b7
Source noteuspto-grants-2011_01