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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511718Generated: October 31, 2026

Triethylamine → 4-(4,4,4-Trifluorobutoxy)phenol

https://huagongshe.com/reaction/511718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(Benzyloxy)-4-(4,4,4-trifluorobutoxy)benzeneHCID 67455899—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-(4,4,4-Trifluorobutoxy)phenolHCID 6745496496.5%

Reaction Steps

60 g (193 mmol) of 1-(benzyloxy)-4-(4,4,4-trifluorobutoxy)benzene, and 7.61 g of Pd/C are dissolved in 900 mL of THF. 5 mL of triethylamine are added to the suspension. The reaction is hydrogenated under atmospheric pressure for 2 hours. The suspension is filtrated of 400 g of hyflo. The organic phase is concentrated under reduced pressure. Filtration of the residue on 900 g silica gel using toluene:ethyl acetate 4:1 as eluent and concentration under reduced pressure yields 41 g of 4-(4,4,4-trifluorobutoxy)phenol as a reddish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09097938B2
Source datasetuspto-grants-2015_08
ORD IDord-ef1aa17e29614c69bf6b09f8c1eaa6b5
Source noteuspto-grants-2015_08