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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582745Generated: October 26, 2026

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

https://huagongshe.com/reaction/582745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTriethylsilaneHCID 12052—
ReactantEthyl aluminium dichlorideHCID 16686341—
Reactant(1RS,4RS)-3-ethyl-4-methyl-4-methoxymethoxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 57024402—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product(RS)-3-ethyl-4-methyl-3-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 5718438153.2%

Reaction Steps

To a solution mixture of 2.35 g of (1RS,4RS)-3-ethyl-4-methyl-4-methoxymethoxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether and 25 ml of dichloromethane was added under nitrogen stream and at -78° C. 1.4 ml of triethylsilane by drops, and the resulting mixture was stirred for 15 minutes. Thereafter, under the same conditions, 8.17 ml of 0.93 M hexane solution of ethylaluminum dichloride was added by drops and the resulting mixture was brought up to -10° C. over 1 hour. Thereafter, the reaction liquid was poured into ice-cooled 5% aqueous solution of citric acid and extracted with diethyl ether. The 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 1 g of (RS)-3-ethyl-4-methyl-3-cyclopenten-1-yl (t-butyldimethylsilyl) ether. Yield 53%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925676
Source datasetuspto-grants-1999_07
ORD IDord-52fe97857a6b493086c4cbb2256f1b10
Source noteuspto-grants-1999_07