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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59712Generated: October 30, 2026

Trifluoromethanesulfonyl chloride → HCID 55256123, compound

https://huagongshe.com/reaction/59712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-3-(pyridin-3-yl)propanoic acidHCID 3606547—
SolventAcetonitrileHCID 6342—
ProductHCID 55256123HCID 5525612342%

Reaction Conditions

Temperature77.5 °C

Reaction Steps

To a mixture of 20.20 g (0.24 mole) sodium bicarbonate (Sigma, Ultrapure, dried in good vacuum at room temperature for 3 days over phosphorus pentoxide) and 6.64 g (0.04 mole) 3-amino-3-(pyridine-3-yl)propionic acid (Tyger, dried in good vacuum at room temperature for 3 days over phosphorus pentoxide) under argon atmosphere first 200 ml of dry acetonitrile (Fisher) was added then at very strong stirring 4.7 ml (0.044 mole) trifluormethanesulfonyl chloride (Acros) was slowly added and thereafter the reaction mixture was further stirred in an oil bath of 75-80° C. for 19 hours. After cooling and stirring in ice bath for 1 hour the reaction mixture was filtered, washed three times with dry acetonitrile and the combined organic solutions were evaporated on a rotavapor at 35° C. The solid residue (23.8 g) was extracted in a Soxhlet-type extractor with boiling chloroform for 26 hours. The evaporation of the chloroform solution gave 2.48 g (42%) pure product as white crystalline material (mp: 115-116° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440948B2
Source datasetuspto-grants-2016_09
ORD IDord-bbf56ee647a448dbb5b19014e52ea0bb
Source noteuspto-grants-2016_09