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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241110Generated: November 4, 2026

Perfluorophenyl 4-(nitrooxy)butanoate → HCID 178441677, compound

https://huagongshe.com/reaction/2241110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluorophenyl 4-(nitrooxy)butanoateHCID 11522541—
ReactantHCID 178441684HCID 178441684—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 178441677HCID 17844167767.3%

Reaction Steps

To a solution of 2-butyl-4-chloro-1-[[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-imidazole-5-methanol (0.48 g, 1.1 mmol), TEA (0.16 ml, 1.1 mmol) and DMAP (0.14 mg, 1.1 mmol) in DMF (3 ml), cooled to 0° C., a solution of 4-nitrooxybutyric acid pentafluorophenyl ester (0.36 g, 1.1 mmol) in DMF (3 ml) was added. The reaction was slowly warmed to room temperature and stirred for 3 hours. Then the solvent was evaporated under reduced pressure. The residue was dissolved in EtOAc (10 ml) and washed with a buffer solution (pH=3) then with brine. The organic layer was dried over Na2SO4, concentrated and purified by flash chromatography (CH2Cl2/MeOH 98:2) to afford the title compound (0.41 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723529B2
Source datasetuspto-grants-2010_05
ORD IDord-cedbdfb37e5143328c6a917d0ff44319
Source noteuspto-grants-2010_05