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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066352Generated: October 30, 2026

Triethylamine → HCID 16070660, compound

https://huagongshe.com/reaction/2066352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantOxt-101HCID 76444—
ReactantSodium BicarbonateHCID 516892—
SolventTolueneHCID 1140—
ProductHCID 16070660HCID 16070660100%

Reaction Steps

After adding 465 g (4.0 mol) of 3-ethyl-3-hydroxymethyloxetane, 486 g (4.8 mol) of triethylamine, and 1840 ml of toluene in a glass flask having an internal volume of 5000 ml equipped with a stirrer, a thermometer, and a dropping funnel, 504 g (4.4 mol) of methanesulfonyl chloride was gently added while keeping the liquid temperature from 5° C. to 10° C. to carry out a reaction, while stirring, at the same temperature range for three hours and at room temperature for three hours. After completing the reaction, 930 ml of a saturated aqueous sodium hydrogen carbonate solution (concentration of 9.3 mass %) was added to the reaction solution to separate into a water layer and an organic layer. Then, after extracting the water layer with 930 ml of toluene, the extract was combined with the previous organic layer and washed with 465 ml of water. By concentrating the organic layer thus obtained under reduced pressure, 777 g of 3-ethyl-3-methanesulfonyloxymethyloxetane with a purity of 95 mass % (quantitative value determined by 1H-NMR) as a brown liquid was obtained (isolated yield based on 3-ethyl-3-hydroxymethyloxetane=95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293448B2
Source datasetuspto-grants-2012_10
ORD IDord-6fe8260796f2475eb383089dd78982d5
Source noteuspto-grants-2012_10