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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028954Generated: November 2, 2026

Lithium Chloride → (2-Bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone

https://huagongshe.com/reaction/1028954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantOxane-4-carbonyl chlorideHCID 2795505—
ReactantPentamethylene-1,5-bis(magnesium bromide)HCID 3637391—
ReactantHCID 178418260HCID 178418260—
ReactantHCID 178419606HCID 178419606—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromophenyl)(tetrahydro-2H-pyran-4-yl)methanoneHCID 63936269—

Reaction Steps

Lithium chloride (0.16 mL, 7.8 mmol) and copper cyanide (0.12 mL, 3.9 mmol) were dissolved in dry THF (4 mL) under nitrogen. This was added dropwise to pentamethylenebis(magnesium bromide) (0.5 M in THF, 7.79 mL, 3.9 mmol) in a dry ice bath under nitrogen and the mixture stirred for 30 min. I-Bromo-2-iodobenzene (0.50 mL, 3.9 mmol) was added and the flask was removed from the cold bath. After 30 min additional dry THF (5 mL) was added and stirred for another 40 min. Then tetrahydro-2H-pyran-4-carbonyl chloride (0.58 mL, 3.9 mmol) was added in one portion, and the mixture was stirred for 15 min. The reaction was quenched by addition of saturated ammonium chloride (10 mL). Ethyl acetate (100 mL) and water (100 mL) were added and the phases were mixed and separated. The organic layer was separated, dried with magnesium sulfate and evaporated to dryness under reduced pressure. Purification using silica column chromatography (hexane to ethyl acetate gradient) gave (2-bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-dff836534f2b4667bc15b944c9965aa3
Source noteuspto-grants-2014_05