HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045338Generated: October 30, 2026
Triethylamine → 4-(2-Methanesulfonylethyl)-2,2-dimethyl-1,3-dioxolane
https://huagongshe.com/reaction/1045338
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(2,2-Dimethyl-1,3-dioxolan-4-yl)ethan-1-ol | HCID 4219754 | — |
| Product | 4-(2-Methanesulfonylethyl)-2,2-dimethyl-1,3-dioxolane | HCID 66898331 | — |
Reaction Steps
4-(2-Hydroxylethyl)-2,2-dimethyl-1,3-dioxolane (25 g, 170 mmol), triethylamine (55.9 mL, 400 mmol), and a stir bar were added to a 1000 mL round bottom flask. The flask was sealed and flushed with nitrogen. Anhydrous DCM (600 mL) was added, and the mixture cooled to approx −5° C. (ice and NaCl). Mesyl chloride (19.9 mL, 255 mmol, 1.5 eq) was added slowly via syringe over a 60 minute period, and the reaction stirred at −5° C. for a further 1.5 hours. At this point TLC showed that the starting material had been consumed. The solution was diluted with DCM (350 mL), divided into two (˜500 mL) portions, and each portion worked up as follows: the solution was transferred to a 1000-mL separating funnel and washed with saturated NaHCO3 (2×200 mL). The organic phase was then dried (MgSO4), filtered, and concentrated (rotovap). The crude product was purified by column chromatography. Final yield: 32.0 g, 84.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569256B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-182dc6d706eb41fdbd0bc38e2506cb37 |
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| Source note | uspto-grants-2013_10 |
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