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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533536Generated: October 30, 2026

Hydrochloric Acid → (+/-)-N-Hydroxy-2-methyl-2-(methylsulfonyl)-4-(4'-nitrobiphenyl-4-yl)butanamide

https://huagongshe.com/reaction/533536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(+/-)-2-Methyl-2-(methylsulfonyl)-4-(4'-nitrobiphenyl-4-yl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamideHCID 86668765—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product(+/-)-N-Hydroxy-2-methyl-2-(methylsulfonyl)-4-(4'-nitrobiphenyl-4-yl)butanamideHCID 5104998687%

Reaction Steps

A solution of HCl in dioxane (4.0 M, 10 mL) was added to a solution of (+/−)-2-methyl-2-(methylsulfonyl)-4-(4′-nitrobiphenyl-4-yl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide (700 mg, 1.47 mmol) in DCM (5 mL) at 0° C. The reaction was warmed to room temperature as the ice bath expired. After 4 hours the reaction was concentrated. Purification on silica by flash column chromatography (DCM/MeOH 99:1-95:5) afforded the title compound as a yellow solid (500 mg, 87%). LCMS m/z 391.1 (M−1). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.57 (s, 3H) 1.87-2.01 (m, 1H) 2.35-2.59 (m, 2H) 2.64-2.80 (m, 1H) 3.05 (s, 3H) 7.41 (d, J=8.20 Hz, 2H) 7.74 (d, J=8.59 Hz, 2H) 7.88-8.06 (m, 2H) 8.22-8.39 (m, 2H) 9.23 (br. s., 1H) 10.98 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853258B2
Source datasetuspto-grants-2014_10
ORD IDord-7b0259eb61f04f1dbc8b4a2d798f604c
Source noteuspto-grants-2014_10