Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77322Generated: October 26, 2026

Triethylamine → Trifluoromethanesulfonate

https://huagongshe.com/reaction/77322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantN-Isoamyl-N-(6-hydroxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 67155390—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTrifluoromethanesulfonateHCID 2758875—
ProductN-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 86653275—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-isoamyl-N-(6-hydroxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (0.18 g, 0.35 mmol) in dichloromethane (10 mL) at 0° C. is added triethylamine (0.099 mL, 0.71 mmol), triflic anhydride (0.089 mL, 0.53 mmol), and 4-dimethylaminopyridine (0.004 g, 0.035 mmol). The reaction is stirred at 0° C. for 1 hour. The solvents are removed in vacuo, and the residue is purified by column chromatography (6% hexanes-ethyl acetate) to afford the title compound (a triflate) as a yellow solid (0.14 g, 68% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841291B2
Source datasetuspto-grants-2014_09
ORD IDord-ff2caca0eef64b8a8e81656a051c760e
Source noteuspto-grants-2014_09