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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582743Generated: October 31, 2026

Citric Acid → (1RS,4RS)-3-ethyl-4-methyl-4-hydroxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether

https://huagongshe.com/reaction/582743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTetrahydrofuranHCID 8028—
Reactant(RS)-3-ethyl-4-oxo-2-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 57084195—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product(1RS,4RS)-3-ethyl-4-methyl-4-hydroxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 5703280898%

Reaction Steps

To a liquid mixture of 2 g of (RS)-3-ethyl-4-oxo-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether and 20 ml of tetrahydrofuran was added under nitrogen stream 10 ml of 1.07 M diethyl ether solution of methyllithium at -78° C. and the resulting mixture was stirred at the same temperature for 2 hours. Then the reaction liquid was poured into ice-cooled 5% aqueous solution of citric acid and extracted two times with diethyl ether. The combined ether layer was washed successively with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, then dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography to obtain 2.1 g of (1RS,4RS)-3-ethyl-4-methyl-4-hydroxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether. Yield 98%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925676
Source datasetuspto-grants-1999_07
ORD IDord-550e275159824f7cbc459f230db1c652
Source noteuspto-grants-1999_07