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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304111Generated: October 27, 2026

((4-Bromobutoxy)methyl)benzene → [(Heptyloxy)methyl]benzene

https://huagongshe.com/reaction/2304111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((4-Bromobutoxy)methyl)benzeneHCID 4422181—
ReactantMagnesiumHCID 5462224—
Reactantp-Fluorophenylglycidyl etherHCID 57037655—
ReactantHCID 178418260HCID 178418260—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
Product[(Heptyloxy)methyl]benzeneHCID 285096—

Reaction Steps

Magnesium (2.4 g, 98 mmol) was added to a 250 ml flask and flame dried. Dry THF, 25 ml, and 1 ml of dibromoethane were then added. 1-Bromo-4-benzyloxy-butane 41 (12 g, 49.4 mmol) dissolved in 50 ml of dry THF was added dropwise and the reaction mixture was stirred at room temperature. After 1 hour, the reaction mixture is cooled in an ice-water bath and 90 mg of copper cyanide is added. After 10 minutes in an ice-bath, 4-fluorophenyl-glycidyl ether (5 g, 29.6 mmol) dissolved in 30 ml of dry THF is added slowly. The reaction is monitored by TLC (ethyl acetate:hexane 3:7). After 15 minutes, the reaction is quenched with saturated aqueous ammonium chloride, concentrated and partitioned between water-ethyl acetate. The ethyl acetate layer is then washed with brine, dried over Na2SO4 and concentrated to give the desired benzyloxy-heptane 42. The structure was confirmed by 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433197B1
Source datasetuspto-grants-2002_08
ORD IDord-246c6cd2426b47d3aa995f1de32a8899
Source noteuspto-grants-2002_08