HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915873Generated: October 31, 2026
Triethylamine → Oxetan-3-ylmethyl methanesulfonate
https://huagongshe.com/reaction/1915873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Oxetan-3-ylmethanol | HCID 11521066 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Oxetan-3-ylmethyl methanesulfonate | HCID 86680078 | — |
Reaction Steps
Oxetan-3-ylmethanol (1.85 g, 21.0 mmol) was dissolved in methylene chloride and cooled to 0° C. Triethylamine (5.31 g, 52.2 mmol) was added followed by slow addition of methanesulfonyl chloride (2.89 g, 25.2 mmol). The mixture was allowed to warm to ambient temperature for 2 h and quenched with sat. sodium bicarbonate (14 mL). The aqueous solution was extracted with methylene chloride 3×. The combined organic layers were dried over sodium sulfate, filtered and concentrated to give crude oxetan-3-ylmethyl methanesulfonate (quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614206B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-3452a4ced46a404d9ad0478512be16b4 |
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| Source note | uspto-grants-2013_12 |
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