HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747182Generated: October 30, 2026
Triethylamine → [3-(4-Bromophenyl)-4,5-dihydroisoxazol-5-yl]methyl methanesulfonate
https://huagongshe.com/reaction/747182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [3-(4-Bromophenyl)-4,5-dihydro-1,2-oxazol-5-yl]methanol | HCID 15888252 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [3-(4-Bromophenyl)-4,5-dihydroisoxazol-5-yl]methyl methanesulfonate | HCID 18698757 | 100.4% |
Reaction Steps
[3-(4-Bromo-phenyl)-4,5-dihydro-isoxazol-5-yl]-methanol (84.3 g, 328 mmol) was added to anhydrous dichloromethane (500 ml) followed by addition of triethylamine (64.1 ml, 459.2 mmol). The solution was allowed to cool to 0° C. followed by dropwise addition of methane sulfonyl chloride (30.65 ml, 396 mmol). The reaction was stirred for 2 hours at 0° C. and then aqueous sodium bicarbonate (200 ml) was added. After further extraction with dichloromethane (2×200 ml), the organic layers were combined, dried over sodium sulfate, and concentrated in vacuo to give the desired product (110 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396847B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-5de72995025d4967b05cf58a32c86df7 |
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| Source note | uspto-grants-2008_07 |
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