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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844576Generated: October 29, 2026

Methanol → HCID 86675622, compound

https://huagongshe.com/reaction/1844576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant(E)-2-PentenalHCID 5364752—
Reactant(S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl EtherHCID 11198150—
SolventNitromethaneHCID 6375—
ProductHCID 86675622HCID 86675622—

Reaction Steps

Nitromethane (4.33 mL) was added to a solution of trans-2-pentenal (2.27 g) and (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine (Org. Lett., 2007, vol. 9, p. 5307) (920 mg) in methanol (54 mL) with stirring at room temperature. The mixture was stirred at room temperature for 4 days. Then, trimethyl orthoformate (17.7 mL) and p-toluenesulfonic acid monohydrate (1.03 g) were added to the reaction solution, and the mixture was further stirred overnight. The reaction solution was concentrated, and a saturated aqueous solution of sodium bicarbonate was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated sodium chloride solution and then dried over anhydrous sodium sulfate. Filtration and concentration under reduced pressure were performed to obtain the title compound (4.81 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946443B2
Source datasetuspto-grants-2015_02
ORD IDord-d1f7c95a0ca44a2289414dd77f13e44e
Source noteuspto-grants-2015_02