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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391766Generated: November 4, 2026

Tributylphosphine → HCID 58629852, compound

https://huagongshe.com/reaction/1391766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 58629819HCID 58629819—
Reactant1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanolHCID 58629822—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58629852HCID 5862985236.7%

Reaction Steps

To a stirred solution of 1-{6-[4-(trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanol (62 mg, 0.20 mmol) and 2-(trimethylsilyl)ethyl 4-(4-hydroxyphenyl)butanoate (55 mg, 0.20 mmol) in dry THF (4 mL) at 0° C. (ice/water bath), under nitrogen, was added ADDP (102 mg, 0.40 mmol) followed by nBu3P (100 μL, 0.40 mmol), and the mixture stirred with slow warming to rt over 64.5 hours. The mixture was then concentrated under vacuum and the solid residue partitioned between DCM (5 mL) and water (5 mL) using a hydrophobic frit. The layers were separated and the aqueous layer re-extracted with DCM (5 mL) and the combined organic layer reduced. Purification by SPE (silica, 5 g Cartridge) eluting with cyclohexane:EtOAc (gradient 50:1 to 7.5:1) afforded the title compound (42 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338960B2
Source datasetuspto-grants-2008_03
ORD IDord-5cd6a0c76808416eb38ff0fd6e549771
Source noteuspto-grants-2008_03