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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889613Generated: October 29, 2026

Allyl bromide → HCID 14297067, compound

https://huagongshe.com/reaction/1889613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant3-PentanolHCID 11428—
ReactantSodium hydrideHCID 24758—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14297067HCID 1429706782.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (60% in oil, 2.76 g, 68.3 mmol) was added to a solution of 3-pentanol (4 g, 45.5 mmol) in tetrahydrofuran (20 mL) at 0° C. under argon atmosphere. The reaction mixture was stirred for 10 min at 0° C. followed by addition of allyl bromide (8.2 g, 68.3 mmol) and tetrabutylammonium iodide (60 mg, 0.016 mmol). The resulting mixture was stirred for 16 hrs at 23° C. before being quenched by addition of a saturated aqueous ammonium chloride solution. The organic layer was extracted with trichloromethane, washed with saturated aqueous sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. Distillation at atmospheric pressure yielded 3-(allyloxy)pentane (compound S1, 4.8 g, yield 82%, boiling point 115° C. to 120° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501980B2
Source datasetuspto-grants-2013_08
ORD IDord-ed6b1f76170e4ba59d1bfe844a2a619e
Source noteuspto-grants-2013_08