HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037702Generated: October 30, 2026
Triethylamine → 3,5-Di-tert-butylphenyl methanesulfonate
https://huagongshe.com/reaction/1037702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,5-Di-tert-butylphenyl methanesulfonate | HCID 86639502 | 98% |
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 1.45 g (0.013 mol) of methanesulfonyl chloride over the course of 10 minutes at 5° C. Following completion of dropping, the mixture was stirred for 3 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 3.21 g (yield: 98%) of 3,5-di-tert-butylphenyl methanesulfonate. A purified product crystallized with n-hexane (white crystals, melting point: 76° C.) was used in a battery test.
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-5cab1da68c044954a2999520c8f9084a |
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| Source note | uspto-grants-2013_10 |
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