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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158465Generated: November 4, 2026

Potassium Carbonate → 4-tert-Butyl-3-(3-methoxy-propoxy)-benzoic acid methyl ester

https://huagongshe.com/reaction/1158465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
Reactant4-tert-Butyl-3-hydroxy-benzoic acid methyl esterHCID 23345341—
SolventAcetonitrileHCID 6342—
Product4-tert-Butyl-3-(3-methoxy-propoxy)-benzoic acid methyl esterHCID 68641350—

Reaction Steps

A mixture of 4-tert-butyl-3-hydroxy-benzoic acid methyl ester (1.56 g, 7.49 mmol), 3-bromopropyl methyl ether (1.72 g, 11.2 mmol) and anhydrous K2CO3 (1.55 g, 11.2 mmol) in MeCN (30 mL) is refluxed overnight. After cooling, the mixture is filtered, the filtrate is diluted with CH2Cl2 and the organics are washed with aqueous 0.5M NaOH, aqueous 0.5M HCl and water, dried (Na2SO4) and concentrated. Purification by flash chromatography on silica gel (hexane/AcOEt 97:3) gives the title compound as colorless oil. MS: 281.1 [M+H]+. tR (HPLC, Nucleosil C18HD column, 5-100% CH3CN/H2O/6 min, 100% CH3CN/2 min, CH3CN and H2O containing 0.1% TFA, flow: 1 mL/min): 6.22 min. 1H-NMR (CDCl3): δ 1.43 (s, 9H), 2.17 (m, 2H), 3.41 (s, 3H), 3.65 (m, 2H), 3.93 (s, 3H), 4.18 (m, 2H), 7.36 (dd, 1H), 7.96 (d, 1H), 7.60 (dd, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-f9d629d8847d4122866a7fbda4c65350
Source noteuspto-grants-2010_10