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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986329Generated: October 26, 2026

Lithium diisopropylamide → 4-Trimethylsilyloxy-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-octyl-2-cyclopentenone

https://huagongshe.com/reaction/986329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl 7-oxoheptanoateHCID 3015770—
Reactant(4R)-4-trimethylsilyloxy-4-octyl-2-cyclopentenoneHCID 13767761—
ReactantIsopropylamideHCID 18378000—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Trimethylsilyloxy-5-(1-hydroxy-6-methoxycarbonylhexyl)-4-octyl-2-cyclopentenoneHCID 13767764—

Reaction Steps

Under a nitrogen atmosphere at -78° C., a solution of 200 mg (0.71 mmole) of (4R)-4-trimethylsilyloxy-4-octyl-2-cyclopentenone in 2 ml of tetrahydrofuran was added to a solution of LDA prepared from 93 mg (0.92 mmole) of isopropylamide and 590 microliters of n-butyllithium (as a 10 W/V % hexane solution) in 3 ml of tetrahydrofuran, and the mixture was stirred for 1 hour. Then, a solution of 146 mg (0.92 mmole) of methyl 6-formylhexanoate in 2 ml of tetrahydrofuran was added, and the mixture was stirred at -78° C. for 2 hours. The reaction was terminated by adding an aqueous solution of ammonium chloride. The reaction mixture was extracted with ether, and the extract was dried over anhydrous magnesium sulfate, filtered and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04711895
Source datasetuspto-grants-1987_12
ORD IDord-5289f19d942d4f9d850c5379261cf8ac
Source noteuspto-grants-1987_12