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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728519Generated: October 30, 2026

Hydrochloric Acid → Benzyl Phenyl Ether

https://huagongshe.com/reaction/728519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1-Bromo-4-phenylmethoxybenzeneHCID 138835—
ReactantSodium BicarbonateHCID 516892—
ReactantMagnesiumHCID 5462224—
ReactantHCID 14139287HCID 14139287—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl Phenyl EtherHCID 7035247%

Reaction Steps

In a 200 ml-volume flask was charged 1 704 g of metallic magnesium. After displacing the atmosphere with nitrogen, a small amount of iodine was added thereto, followed by heating to activate the magnesium. Ten milliliters of tetrahydrofuran (THF) were added thereto, and a mixture comprising 18.5 g of 4-bromophenyl benzyl ether as prepared in Example 1 and 40 ml of THF was added dropwise to the system from a dropping funnel at room temperature over a period of 30 minutes. The reaction was continued at a refluxing temperature of THF for an additional 2.5 hours to prepare a Grignard reagent. To the resulting Grignard reagent was added a mixture of 10.0 g of (S)-2,6-dimethylheptanal and 30 ml of THF at 15° C., followed by allowing the mixture to react for 2 hours while keeping at that temperature. The reaction mixture was treated with diluted hydrochloric acid, neutralized with a sodium bicarbonate aqueous solution, and washed with water to obtain 21.8 g of a crude product. Purification by silica gel column chromatography (eluent: benzene) yielded 11.8 g (theoretical yield: 47%) of the entitled compound as a viscous yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049308
Source datasetuspto-grants-1991_09
ORD IDord-3b76e8062ca7487c974a0f043b1d7cf6
Source noteuspto-grants-1991_09