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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253360Generated: October 31, 2026

Sodium hydride → HCID 59659237, compound

https://huagongshe.com/reaction/253360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
ReactantHCID 59659186HCID 59659186—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 59659237HCID 59659237—

Reaction Steps

At room temperature, 12 mg of a 60 percent strength sodium hydride suspension are added to a suspension of 55 mg of trimethylsulfonium iodide in 2 ml of DMSO, and the mixture is stirred at room temperature for 20 min. At 10° C., 100 mg of ethyl (1R,3S)-2-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxymethyl]acrylate, dissolved in 2 ml of DMSO, are then added, and the mixture is stirred at room temperature for 90 min. The mixture is poured into ice-water and extracted with methyl tert-butyl ether. The organic phase is dried over sodium sulfate, the solvent is removed under reduced pressure and the residue is purified by flash chromatography on silica gel (n-heptane/ethyl acetate=2:1). This gives ethyl (1R,3S)-1-[3-(5-methyl-2-m-tolyloxazol-4-ylmethoxy)cyclohexyloxymethyl]cyclopropanecarboxylate as a colorless oil. C25H33NO5 (427.55), MS (ESI): 428 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872034B2
Source datasetuspto-grants-2011_01
ORD IDord-2029a895678149a5bceefe9e6b7f0eda
Source noteuspto-grants-2011_01