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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725203Generated: October 26, 2026

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

https://huagongshe.com/reaction/1725203

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 numberUS07488848B2
Source datasetuspto-grants-2009_02
ORD IDord-9fd18a8643f746cc8eb3610da1235ff4
Source noteuspto-grants-2009_02