HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355271Generated: October 27, 2026
Triethylamine → 4-Methylsulfonyloxymethyl-1,3-dioxane
https://huagongshe.com/reaction/355271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (1,3-Dioxan-4-yl)methanol | HCID 13976559 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methylsulfonyloxymethyl-1,3-dioxane | HCID 18941616 | 67.3% |
Reaction Steps
A stirred solution of 16.2 grams (0.137 mole) of 1,3-dioxan-4-ylmethanol and 16.7 grams (0.165 mole) of triethylamine in 250 mL of methylene chloride was cooled to about -20° C., and a solution of 17.3 grams (0.151 mole) of methanesulfonyl chloride in about 25 mL of methylene chloride was added dropwise. Upon completion of addition the reaction mixture was allowed to warm to ambient temperature as it stirred for one hour. The reaction mixture was then washed with water and dried with magnesium sulfate. The mixture was filtered and concentrated under reduced pressure to a residue. The residue was purified using column chromatography on silica gel, yielding 18.1 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0001759 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-18e8703d02b2465b8467d4e10992f5b4 |
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| Source note | uspto-grants-1998_11 |
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