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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037698Generated: October 25, 2026

2,4-Di-tert-butylphenol → 2,4-Di-tert-butylphenyl methanesulfonate

https://huagongshe.com/reaction/1037698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Di-tert-butylphenolHCID 7311—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
Product2,4-Di-tert-butylphenyl methanesulfonateHCID 4454271690%

Reaction Conditions

Temperature25 °C

Reaction Steps

21.00 g (0.102 mol) of 2,4-di-tert-butylphenol and 11.84 g (0.117 mol) of triethylamine were dissolved in 200 mL of toluene followed by dropping in 12.24 g (0.107 mol) of methanesulfonyl chloride over the course of 30 minutes at 10° C. Following completion of dropping, the mixture was stirred for 2 hours at 25° C. and the 2,4-di-tert-butylphenol was confirmed to no longer be present. The reaction liquid was placed in 3% aqueous hydrochloric acid solution and following separation of the organic layer, was washed once with saturated aqueous NaHCO3 solution and twice with saturated brine followed by drying with MgSO4 and concentrating. The resulting crude crystals were purified by crystallization with n-heptane to obtain 25.8 g (yield: 90%) of 2,4-di-tert-butylphenyl methanesulfonate (white crystals, melting point: 63° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546599B2
Source datasetuspto-grants-2013_10
ORD IDord-e5df211c89ad46a4a4232bdf09759a43
Source noteuspto-grants-2013_10