Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700896Generated: October 27, 2026

1,1,1-Trifluorobut-3-en-2-ol → 3-[N-Dodecyl-N-2-[4-(E)-[3-hydroxy-4,4,4-trifluorobut-1-en-1-yl]phenoxy]ethylamino]propanoic Acid, Ethyl Ester

https://huagongshe.com/reaction/1700896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluorobut-3-en-2-olHCID 13262956—
Reactant4-[N-dodecyl-N-2-[4-(E)-[3-hydroxy-4,4,4-trifluorobut-1-en-1-yl]phenoxy]ethylamino] butanoic acid, ethyl esterHCID 86757121—
Reactant[N-Dodecyl-N-[2-[4-iodophenoxy]ethyl]amino]propanoic acid, ethyl esterHCID 86757125—
Product3-[N-Dodecyl-N-2-[4-(E)-[3-hydroxy-4,4,4-trifluorobut-1-en-1-yl]phenoxy]ethylamino]propanoic Acid, Ethyl EsterHCID 8675712476%

Reaction Steps

[N-Dodecyl-N-[2-[4-iodophenoxy]ethyl]amino]propanoic acid, ethyl ester (0.95 g, 1.79 mmol) and 4,4,4-trifluorobut-1-en-3-ol (complex with 0.7 THF, 0.95 g, 5.4 mmol) were reacted by the general procedure as described in the preparation of 4-[N-dodecyl-N-2-[4-(E)-[3-hydroxy-4,4,4-trifluorobut-1-en-1-yl]phenoxy]ethylamino]butanoic acid, ethyl ester (Example 48) and afforded the title compound (0.633 g, 76%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-957a81e85b654ca895c9d95f5ba73eca
Source noteuspto-grants-2002_02