Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582741Generated: October 26, 2026

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

https://huagongshe.com/reaction/582741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTriethylsilaneHCID 12052—
ReactantEthyl aluminium dichlorideHCID 16686341—
Reactant(1RS,4RS)-3-allyl-4-methyl-4-methoxymethoxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 57042147—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product(RS)-3-allyl-4-methyl-3-cyclopenten-1-yl (t-butyldimethylsilyl) etherHCID 5703887755%

Reaction Steps

To a solution mixture of 4.5 g of (1RS,4RS)-3-allyl-4-methyl-4-methoxymethoxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether and 50 ml of dichloromethane was added under nitrogen stream 3 ml of triethylsilane by drops at -78° C., and the resulting mixture was stirred for 15 minutes. Thereafter, under the same conditions, 17.5 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. Then 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 2 g of (RS)-3-allyl-4-methyl-3-cyclopenten-1-yl (t-butyldimethylsilyl) ether. Yield 55%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925676
Source datasetuspto-grants-1999_07
ORD IDord-a8eeb8643a7e417a8bbbb2fc5a71de42
Source noteuspto-grants-1999_07