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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,4-Di-tert-butylphenyl methanesulfonate | HCID 44542716 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546599B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-e5df211c89ad46a4a4232bdf09759a43 |
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| Source note | uspto-grants-2013_10 |
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