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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774686Generated: October 30, 2026

Water → HCID 89435495, compound

https://huagongshe.com/reaction/1774686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-DodecanolHCID 8193—
ReactantSodium hydrideHCID 24758—
ReactantHCID 117855853HCID 117855853—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89435495HCID 8943549539.5%

Reaction Steps

1-Dodecanol (0.10 g) was dissolved in anhydrous THF (5 ml) under a nitrogen atmosphere and sodium hydride (about 55% oil) (25 mg) was added under ice-cooling with stirring. The reaction mixture was stirred at room temperature for 30 min under a nitrogen atmosphere, and then the mixture was ice-cooled. To the mixture was added a solution (5 ml) of carbonic acid 7-[4-(4-benzo[b]thiophen-4-ylpiperazin-1-yl)butoxy]-2-oxo-2H-quinolin-1-ylmethyl ester 4-nitrophenyl ester obtained in Example 133 (0.33 g) in anhydrous THF using a cannula. Under a nitrogen atmosphere, the reaction mixture was stirred with ice-cooling for 2 hr, and at room temperature for 1 hr. Water was added to the reaction mixture to discontinue the reaction, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated by filtration. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to give the title compound (0.14 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260420B2
Source datasetuspto-grants-2016_02
ORD IDord-dd04e76cdc8a43ac9dc977e1c66dbb7d
Source noteuspto-grants-2016_02