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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377132Generated: October 26, 2026

Hexane → (3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanol

https://huagongshe.com/reaction/2377132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-methyl-1H-1,2,3-benzotriazole-5-carbaldehydeHCID 2795417—
Reactant4-Bromo-2-ethoxy-1-methoxybenzeneHCID 21772690—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
Product(3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanolHCID 68939793106.4%

Reaction Steps

To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (1.5 g, 6.5 mmol) in THF (15 mL) was added a solution of n-butyllitium in hexane (2.5 mL, 2.5 N, 6.3 mmol) at −78° C. and kept for 20 min. To the mixture was added a slurry of 1-methyl-1H-benzotriazole-5-carbaldehyde (1.0 g, 6.0 mmol) in THF (5 mL) at −78° C. After 18 h, isopropanol (2 mL) and water (10 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent gave (3-ethoxy-4-methoxy-phenyl)-(1-methyl-1H-benzotriazol-5-yl)-methanol as an oil (2 g). The oil was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468446B2
Source datasetuspto-grants-2008_12
ORD IDord-8aec90f965a646ae91c6322b0303dde2
Source noteuspto-grants-2008_12