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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35490Generated: October 28, 2026

Acetic Acid → HCID 56612422, compound

https://huagongshe.com/reaction/35490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 56638654HCID 56638654—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 56612422HCID 5661242279.3%

Reaction Steps

63 mg (0.133 mmole) of 4-(3-t-butyldimethylsilyloxy-3-cyclopentyl-1-propenyl)-5-(1-hydroxy-6-methoxycarbonyl-2-hexyn-1-yl)-2-cyclopentenone obtained in Example 25 was dissolved in 2 ml of a mixed solvent composed of acetic acid, tetrahydrofuran and water in a ratio of 3:2:2, and the solution was stirred for 20 hours. An aqueous solution of sodium bicarbonate and ethyl acetate were added to the reaction mixture to perform extraction. The organic layers were combined, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The dried product was filtered, concentrated and subjected to silica gel column chromatography (silica gel 5 g; eluent, hexane:ethyl acetate=5:1→1:1) to give 38 mg (yield 79%) of 4-(3-hydroxy-3-cyclopentyl-1-propenyl)-5-(1-hydroxy-6-methoxycarbonyl-2-hexyn-yl)-2-cyclopentenone. The resulting compound had the following spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766147
Source datasetuspto-grants-1988_08
ORD IDord-47c58977230c4fd7967d76880a7aea2c
Source noteuspto-grants-1988_08