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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977898Generated: October 31, 2026

Triethylamine → HCID 13822973, compound

https://huagongshe.com/reaction/977898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamideHCID 13822972—
SolventDichloromethaneHCID 6344—
ProductHCID 13822973HCID 13822973—

Reaction Conditions

Temperature0 °C

Reaction Steps

The alcohol from Example 1 (33.1 g) and 20 ml of triethylamine were dissolved in 350 ml of dichloromethane, cooled to 0° C., and treated with 11 ml methanesulfonyl chloride. After being stirred at room temperature for about 20 hours, the reaction mixture was diluted with dichloromethane (100 ml) and the organic layer was washed with three 50-ml portions of water and one of brine. Drying and concentration in vacuo gave the crude product which gradually crystallized upon standing. The solid was washed with diethyl ether, filtered, and dried to yield 12.0 g of 2-[2-(methylsulfonyloxy)ethyl]-N-(1,1-dimethylethyl)benzenesulfonamide as a white powder; m.p. 106°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04662933
Source datasetuspto-grants-1987_05
ORD IDord-596babbebc2d431194fb27bb7f10e09f
Source noteuspto-grants-1987_05