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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172241Generated: October 30, 2026

3-(Trifluoromethyl)phenol → HCID 70873561, compound

https://huagongshe.com/reaction/2172241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 4-(3-hydroxypropyl)tetrahydro-1(2h)-pyridinecarboxylateHCID 2800739—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70873561HCID 7087356186%

Reaction Steps

4-(3-Hydroxypropyl)piperidine-1-carboxylic acid tert-butyl ester (15.0 g, 61.6 mmol), 3-trifluoromethylphenol (19.4 g, 64.7 mmol), triphenylphosphine (1.40 g, 73.9 mmol) and tetrahydrofuran (200 ml) were mixed. While stirring the mixture at room temperature, DEAD (21.1 ml, 80.0 mmol) was added thereto dropwise and heated at reflux for 2 days. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate. After filtering, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=87:13) to afford the title compound as a pale yellow oil (20.5 g, yield 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-3de20a27bdad4bbe86286613e201c5a5
Source noteuspto-grants-2015_06