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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391784Generated: November 3, 2026

Tributylphosphine → HCID 58629891, compound

https://huagongshe.com/reaction/1391784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 19361036HCID 19361036—
Reactant1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanolHCID 58629822—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58629891HCID 5862989134.2%

Reaction Steps

A stirred solution of 1-{6-[4-(trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanol (62 mg, 0.20 mmol) and ethyl (2E)-3-(4-hydroxy-3,5-dimethylphenyl)-2-propenoate (79 mg, 0.36 mmol) in THF (4 mL) at 0° C. under nitrogen was added ADDP (101 mg, 0.40 mmol) followed by tri-N-butylphosphine (0.100 mL, 0.40 mmol). The resulting mixture was then allowed to warm slowly to ambient temperature overnight. After 66 h the solvent was removed under vacuum (Genevac) and the resulting solid partitioned between DCM (5 mL) and water (5 mL), the layers separated and the aqueous re-extracted with DCM (5 mL). The combined organic layer was then reduced under vacuum and purified by SPE (silica, 10 g cartridge) eluting with cyclohexane:EtOAc (gradient 20:1 to 1:1) to give the title compound (35 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338960B2
Source datasetuspto-grants-2008_03
ORD IDord-1938df07b3d3446c92b428ddfd36ba34
Source noteuspto-grants-2008_03