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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744913Generated: October 28, 2026

Hexane → HCID 22226108, compound

https://huagongshe.com/reaction/1744913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantethyl (E)-3-(3-n-propoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-2-fluoropent-2-enoateHCID 86593752—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22226108HCID 22226108—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of diisobutylaluminum hydride and hexane (40 mL, 1 M, 40 mmol) was added to a stirring solution of ethyl (E)-3-(3-n-propoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-2-fluoropent-2-enoate (Intermediate 8, 3.52 g, 9.36 mmol) in THF (60 mL) at −78° C. under argon. The solution was stirred at −78° C. for 3 h, and the reaction was quenched at −78° C. by adding methanol. The solution was warmed to room temperature and stirred for 1.5 h. The solution was treated with 1 M aqueous HCl, and the products were extracted three times with ether. The combined organic layers were washed with water, brine and dried over magnesium sulfate. The solvent was removed in vacuo to give the title compound after purification by silica gel chromatography (15% ethyl acetate in hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019034B2
Source datasetuspto-grants-2006_03
ORD IDord-e3151f77ef8147949ba5296e949ae547
Source noteuspto-grants-2006_03