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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16225Generated: October 25, 2026

4-Pentenal → 1,8-Nonadien-5-ol

https://huagongshe.com/reaction/16225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PentenalHCID 16418—
ReactantHCID 178418797HCID 178418797—
SolventTetrahydrofuranHCID 8028—
Product1,8-Nonadien-5-olHCID 11829542—

Reaction Steps

3-Butenyl-magnesium bromide (125 mL, 0.5 M in tetrahydrofuran, 62.5 mmol) was added drop wise to a stirred and cooled (−78° C.) solution of pent-4-enal (4 g, 48.07 mmol) in dry tetrahydrofuran (160 mL). After the addition, the solution was warmed to room temperature and then quenched with NH4Cl solution. The mixture was partitioned with diethyl ether and the organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. The residue was purified over silica gel using 5-15% diethyl ether in hexanes to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737137B2
Source datasetuspto-grants-2010_06
ORD IDord-e98f6149fafa44c789cdbd4327d485dc
Source noteuspto-grants-2010_06