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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093123Generated: November 2, 2026

Tetrahydrofuran → HCID 68793042, compound

https://huagongshe.com/reaction/2093123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-BromononaneHCID 12742—
ReactantSodium hydrideHCID 24758—
Reactant2-ThiopheneethanolHCID 79400—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68793042HCID 6879304260.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

17 g of 2-thiopheneethanol was cooled to 0° C., and to this, a suspension formed by adding 7.1 g of sodium hydride (60% in oil) to 110 ml of tetrahydrofuran was added dropwise. The solution was stirred at 0° C. for 20 minutes under a nitrogen atmosphere, and to this, 27 g of 1-bromononane was added dropwise. The resulting solution was heated to 90° C. and stirred for 8 hours. 100 ml of water and 100 ml of dichloromethane were added to the reaction solution to separate the organic layer. The organic layer was washed with 300 ml of saturated salt water and then dried over anhydrous magnesium sulfate. The resulting solution was concentrated by a rotary evaporator and purified by a column chromatography (filler: silica gel, eluent: hexane/dichloromethane) to obtain 20 g of 2-(2-nonyloxyethyl)thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08441002B2
Source datasetuspto-grants-2013_05
ORD IDord-1a026891220e49569f33260c14736b27
Source noteuspto-grants-2013_05