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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636076Generated: October 31, 2026

4-(Benzyloxy)-3-methoxybenzaldehyde → HCID 11067615, compound

https://huagongshe.com/reaction/1636076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)-3-methoxybenzaldehydeHCID 75506—
ReactantHCID 178418336HCID 178418336—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11067615HCID 11067615—

Reaction Steps

A solution of 20 g (82.64 mmol) of O-benzylvanillin in 200 mL of dry tetrahydrofuran was slowly added to a stirred solution of benzyl magnesium chloride (103.30 mmol) in 150 mL of diethylether at 10° C. over 20 min, and the reaction mixture was then boiled for 10 min, cooled, quenched with a mixture of ice and dilute hydrochloric acid and evaporated at reduced pressure. The residue was dissolved in dichloromethane, the solution washed with brine, dried with sodium sulphate and the solvent was evaporated under reduced pressure leaving a crystalline residue that was recrystallised from diethylether and petroleum ether. 1-(4-Benzyloxy-3-methoxyphenyl)-2-phenyl-1-ethanol was obtained as white crystals, m.p. 97 to 98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512136B1
Source datasetuspto-grants-2003_01
ORD IDord-42a9c01f1d6745ec82b8d496b2bc87a6
Source noteuspto-grants-2003_01