Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012702Generated: October 30, 2026

Triethylamine → 4-(4-Morpholinylcarbonyl)phenyl trifluoromethanesulphonate

https://huagongshe.com/reaction/1012702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant(4-Hydroxyphenyl)(morpholino)methanoneHCID 7586556—
SolventDichloromethaneHCID 6344—
Product4-(4-Morpholinylcarbonyl)phenyl trifluoromethanesulphonateHCID 17982865—

Reaction Conditions

Temperature-10 °C

Reaction Steps

1.23 ml (7.24 mmol) of trifluoromethanesulphonic anhydride are slowly added dropwise to a solution, cooled to −10° C., of 1.0 g (4.83 mmol) of 4-(4-morpholinylcarbonyl)phenol and 2.02 ml (14.48 mmol) of triethylamine in 20 ml of dichloromethane. The mixture is stirred at −10° C. for 30 min and then at 0° C. for 30 min. It is washed successively with 10% strength sodium bicarbonate solution, water and saturated sodium chloride solution, dried over sodium sulphate and concentrated in vacuo, and the residue is dried under high vacuum. 1.71 g (94.6% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977485B2
Source datasetuspto-grants-2011_07
ORD IDord-606698efdf6a4407bb74b88ebb47cbb7
Source noteuspto-grants-2011_07