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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037703Generated: October 26, 2026

Triethylamine → 3,5-Di-tert-butylphenyl ethanesulfonate

https://huagongshe.com/reaction/1037703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant3,5-Di-tert-butylphenolHCID 70825—
SolventTolueneHCID 1140—
Product3,5-Di-tert-butylphenyl ethanesulfonateHCID 8663950391.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

2.50 g (0.012 mol) of 3,5-di-tert-butylphenol and 1.27 g (0.013 mol) of triethylamine were dissolved in 15 mL of toluene followed by dropping in 1.62 g (0.013 mol) of ethanesulfonyl chloride over the course of 10 minutes at 5° C. Following completion of dropping, the mixture was stirred for 2 hours at 25° C. and the 3,5-di-tert-butylphenol was confirmed to no longer be present. The reaction liquid was placed in ice water and following separation of the organic layer, was washed twice with saturated brine followed by drying with MgSO4 and concentrating to obtain 3.27 g (yield: 91%) of 3,5-di-tert-butylphenyl ethanesulfonate. A purified product crystallized with n-hexane (white crystals, melting point: 52° C.) was used in a battery test.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546599B2
Source datasetuspto-grants-2013_10
ORD IDord-fe98c886bdab41f09ffa4b4644d7af53
Source noteuspto-grants-2013_10