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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598708Generated: October 28, 2026

Triethylamine → N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide

https://huagongshe.com/reaction/598708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-tert-Butyl-2,6-diaminoanisoleHCID 4177235—
SolventDichloromethaneHCID 6344—
ProductN-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamideHCID 1021471087.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an oven dried 250 mL round bottom flask containing 5.0 g (25.73 mmol) 5-tert-butyl-2-methoxy-benzene-1,3-diamine, 150 mL DCM was added. The reaction mixture was cooled to 0° C. after which triethylamine (5.0 mL, 36.0 mmol) was added followed by the drop wise addition of methylsulfonyl chloride (1.99 mL, 25.7 mmol). The reaction was allowed to stir at 0° C. for 30 min. then warmed to room temperature stirring for an additional 2 h. The reaction mixture was poured over saturated solution of sodium bicarbonate (100 mL) and the layers separated. The aqueous layer was washed twice more with 50 mL dichloromethane and the combined organic layers were dried over magnesium sulfate and concentrated under vacuum to afford a crude oil that was purified by flash chromatography (silica gel, 1:1 EtOAc:Hex) to yield 6.1 g of the desired product (87%). Calculated mass=272. Observed mass=273

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897599B2
Source datasetuspto-grants-2011_03
ORD IDord-a4059456a0cb40a6946a821105f41241
Source noteuspto-grants-2011_03