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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Ethyl aluminium dichloride | HCID 16686341 | — |
| Reactant | (1RS,4RS)-3-ethyl-4-methyl-4-methoxymethoxy-2-cyclopenten-1-yl (t-butyldimethylsilyl) ether | HCID 57024402 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (RS)-3-ethyl-4-methyl-3-cyclopenten-1-yl (t-butyldimethylsilyl) ether | HCID 57184381 | 53.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05925676 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-52fe97857a6b493086c4cbb2256f1b10 |
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| Source note | uspto-grants-1999_07 |
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