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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821672Generated: October 31, 2026

2-Tert-Butylphenol → HCID 57486422, compound

https://huagongshe.com/reaction/1821672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-ButylphenolHCID 6923—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57486422HCID 5748642282.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

In dry tetrahydrofuran (25 mL) was suspended 4.80 g (120 mmol) of 60% sodium hydride, and a dry tetrahydrofuran (80 mL) solution containing 15.0 g (100 mmol) of 2-tert-butylphenol was added dropwise to this suspension at 0° C. After stirring the mixture at 0° C. for 10 minutes, a dry tetrahydrofuran (80 mL) solution containing 14.9 g (119 mmol) of 2-methoxyethoxymethyl chloride was added dropwise to the mixture. The reaction mixture was stirred in an ice bath for 4 hours and 30 minutes, and allowed to stand at room temperature overnight. To the reaction mixture were further added 1.20 g (30 mmol) of 60% sodium hydride and 3.8 g (30 mmol) of 2-methoxyethoxymethyl chloride at 0° C., and the mixture was stirred at 0° C. for 7 hours. The reaction mixture was poured into ice-cold water (250 mL), and extracted with ethyl acetate. The organic layers were combined, washed with 2N aqueous sodium hydroxide solution and brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (eluted with hexane:ethyl acetate=20:1) to obtain 19.7 g (82.8 mmol, Yield: 82.8%) of tert-butyl-2-[(2-methoxyethoxy)methoxy]benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-917ccc62768446d995c452e18a0ad0e8
Source noteuspto-grants-2009_10