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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585478Generated: November 3, 2026

Tetrahydrofuran → HCID 15434404, compound

https://huagongshe.com/reaction/1585478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 21218592HCID 21218592—
CatalystAdams' catalystHCID 345198—
SolventEthyl AcetateHCID 8857—
ProductHCID 15434404HCID 1543440482%

Reaction Steps

A solution of 3-[[5-chloro-2-[[[[bis-(phenylmethyl)phosphonooxy]methyl]carbonyl]oxy]phenyl]methyl]-5-[4-(trifluoromethyl)phenyl]- 1,3,4 -oxadiazol-2(3H)-one (138 mg, 0.20 mmol) in ethyl acetate (30 mL) and PtO2 (30 mg) was hydrogenated at 30 psi in a Parr apparatus for 1 hr. After hydrogenation is complete, THF (30 mL) was added to solublize the product and then filtered through a pad of Celite to remove the catalyst. The filtrate was evaporated and the residue was recrytallized twice from ether-hexanes and then acetone-hexanes to afford the title compound as a white powder (83 mg, 82%). MS m/e 509 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939405
Source datasetuspto-grants-1999_08
ORD IDord-c901092fb92340b3b16a61d45b173a81
Source noteuspto-grants-1999_08