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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015974Generated: October 31, 2026

Triethylamine → HCID 15606012, compound

https://huagongshe.com/reaction/1015974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,3-Dioxolane-2,2-diethanolHCID 576020—
SolventDichloromethaneHCID 6344—
ProductHCID 15606012HCID 15606012—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 2,2′-(1,3-dioxolane-2,2-diyl)diethanol (1.3 g, 8.0 mmol) in methylene chloride (100 mL) was added triethylamine (3.4 mL, 24 mmol) at room temperature. The solution was cooled down to −40° C. and then mesyl chloride (1.65 mL, 20 mmol) was added dropwise. The reaction mixture was stirred at −40° C. for 30 min, then warmed up to 0° C. gradually. The reaction was quenched with saturated aqueous NaHCO3 solution. The aqueous layer was extracted with methylene chloride. The combined organic extracts were washed with brine, dried over Na2SO4, then evaporated to afford the crude product, 1,3-dioxolane-2,2-diyldiethane-2,1-diyl dimethanesulfonate: MS (m/e): 319 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985730B2
Source datasetuspto-grants-2011_07
ORD IDord-cbad912478a84acfad97fee052636008
Source noteuspto-grants-2011_07