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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098229Generated: October 26, 2026

2,2,3,3,3-Pentafluoropropanol → 2(R)-(2,2,3,3,3-pentafluoropropylamino)-3-tritylsulfanylpropionic acid

https://huagongshe.com/reaction/2098229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,3,3,3-PentafluoropropanolHCID 9872—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantS-Trityl-L-CysteineHCID 76044—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
Product2(R)-(2,2,3,3,3-pentafluoropropylamino)-3-tritylsulfanylpropionic acidHCID 86610097—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a −78° C. methylene chloride solution (75 mL) of 2,2,3,3,3-pentafluoropropan-1-ol (1.5 g, 10.0 mmol) and DIPEA (6.1 mL, 35.0 mmol) was added triflic anhydride (1.78 mL, 10.5 mmol). After 2.5 h, S-tritylcysteine was added all at once and the reaction mixture was stirred at 0° C. for 80 min. The reaction mixture was stirred at RT for 18 h and then concentrated on the rotovap. Ethyl acetate was added and the reaction mixture was washed with 1N HCl. The organic layer was dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromatography (3 hexanes/1 ethyl acetate+1% acetic acid) to provide 2(R)-(2,2,3,3,3-pentafluoropropylamino)-3-tritylsulfanylpropionic acid (3.29 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450373B2
Source datasetuspto-grants-2013_05
ORD IDord-c7a1b95d23bd42fa84e1f7d8d33e6266
Source noteuspto-grants-2013_05