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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,5-Di-tert-butylphenyl ethanesulfonate | HCID 86639503 | 91.3% |
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
| 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-fe98c886bdab41f09ffa4b4644d7af53 |
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| Source note | uspto-grants-2013_10 |
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