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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264511Generated: November 2, 2026

Sodium Chloride → HCID 19036578, compound

https://huagongshe.com/reaction/264511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantChloroacetoneHCID 6571—
ReactantDiisopropylamineHCID 7912—
Reactant5-Methoxyindan-1-oneHCID 78787—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19036578HCID 1903657856%

Reaction Steps

A lithium diisopropylamide solution, freshly prepared from 4.25 ml of diisopropylamine and 18.7 ml of 1.6N n-butyllithium in hexane, in 60 ml of anhydrous tetrahydrofuran was added dropwise while stirring to a solution, cooled to -70°, of 3.24 g of 5-methoxy-1-indanone in 350 ml of anhydrous tetrahydrofuran. The mixture was stirred at this temperature for an additional 30 minutes and a solution of 1.6 ml of chloroacetone dissolved in 60 ml of anhydrous tetrahydrofuran was subsequently added dropwise over 15 minutes. The reaction mixture was left to come to room temperature over 100 minutes and was stirred at this temperature for an additional 45 minutes. Subsequently, the reaction mixture was poured on to 150 ml of ice, 150 ml of saturated sodium chloride were added and the organic phase was separated. The aqueous phase was extracted once with 400 ml of diethyl ether. The combined organic phases were washed once with 100 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated in a vacuum. The red oil obtained was purified by column chromatography on silica gel (hexane/diethyl ether 3:7). There were obtained 1.67 g of crude product which was crystallized from diethyl ether/hexane. The crystallization gave 1.21 g (56%) of (RS)-5-methoxy-2-(2-oxopropyl)-1-indanone as a light yellow solid with m.p. 73°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-53c9cdedd22d4402bce2103e0b94ac94
Source noteuspto-grants-1997_07