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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190471Generated: October 31, 2026

Water → Methyl 3-[(1,1-dimethylprop-2-yn-1-yl)oxy]benzoate

https://huagongshe.com/reaction/2190471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMethyl 3-HydroxybenzoateHCID 88068—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-[(1,1-dimethylprop-2-yn-1-yl)oxy]benzoateHCID 7633322928%

Reaction Steps

To a solution of methyl 3-hydroxybenzoate (10.0 g, 65.7 mmol) in acetonitrile (200 mL) were added 3-chloro-3-methylbut-1-yne (20.0 g, 195 mmol) and copper (II) chloride (88 mg, 0.654 mmol) under ice-cooling, and the mixture was stirred for 15 min under ice-cooling. 1,8-Diazabicyclo[5.4.0]undec-7-ene (10 mL, 70.0 mmol) was added under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was poured into water (300 mL), and the mixture was extracted with ethyl acetate (400 mL×2). The ethyl acetate layers were combined, and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/0→0/100) to give the title compound (4.0 g, 28%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-986ffb9c5e014644beec986db52d2ec8
Source noteuspto-grants-2012_12