Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403383Generated: October 29, 2026

Morpholine → Methyl 3-(morpholinosulfonyl)-5-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/403383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-(chlorosulfonyl)-5-(trifluoromethyl)benzoateHCID 62631505—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(morpholinosulfonyl)-5-(trifluoromethyl)benzoateHCID 70663402—

Reaction Steps

To an ice-cold solution of methyl 3-(chlorosulfonyl)-5-(trifluoromethyl)benzoate (1.0 g, 3.3 mmol, Buttpark Ltd.) in dichloromethane (10 mL) was added N-ethyldiisopropylamine (854 mg, 1.15 mL, 6.61 mmol) and morpholine (317 mg, 317 μL, 3.63 mmol). The reaction mixture was stirred at room temperature for 2 hours, poured on 10% aqueous sodium bicarbonate solution (100 mL) and dichloromethane (100 mL) and the layers were separated. The aqueous layer was extracted a second time with dichloromethane (100 mL). The organic layers were washed with brine (100 mL), dried over magnesium sulfate, filtered and concentrated under vacuum. The compound was purified by silica gel chromatography on a 20 g column using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate (100:0 to 35:65). Off-white solid (1.04 g, 89%). MS (EI): m/z=353.087 ([M]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748434B2
Source datasetuspto-grants-2014_06
ORD IDord-9401dd491c1543069b9bd98d2360d322
Source noteuspto-grants-2014_06