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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322902Generated: October 26, 2026

Hydrochloric Acid → (R)-4-(2-methylphenyl)-4-(2-nitro-5-(3-pyridylmethoxy)phenoxy)butanoic acid

https://huagongshe.com/reaction/322902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl (R)-4-(2-methylphenyl)-4-(2-nitro-5-(3-pyridylmethoxy)phenoxy)butanoateHCID 53646282—
SolventMethanolHCID 887—
SolventPentaneHCID 8003—
Product(R)-4-(2-methylphenyl)-4-(2-nitro-5-(3-pyridylmethoxy)phenoxy)butanoic acidHCID 5416975521.2%

Reaction Steps

A solution of tert-butyl (R)-4-(2-methylphenyl)-4-(2-nitro-5-(3-pyridylmethoxy)phenoxy)butanoate (800 mg) in methanol (20 mL) containing 5 N sodium hydroxide (10 mL) is stirred at ambient temperature for 48 hours. The reaction mixture is poured into water (50 mL), acidified to pH 5 with 1 N HCl and extracted three times with ethyl acetate (50 mL). The combined organic phases are washed with brine (50 mL), dried over magnesium sulphate, filtered and concentrated under reduced pressure The residual brown gum is purified by flash chromatography on silica eluting with ethyl acetate. Fractions homogeneous in the required product are combined and evaporated to give a yellow oil. Trituration with pentane afforded (R)-4-(2-methylphenyl)-4-(2-nitro-5-(3-pyridylmethoxy)phenoxy)butanoic acid as a white solid (150 mg), m.p. 117-119° C. [Elemental analysis:- C,65.4, H, 5.21, N, 6.64%. Calculated:- C,65.3, H, 5.17, N, 6.59%]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211234B1
Source datasetuspto-grants-2001_04
ORD IDord-228863ac08974c198ad0a97e112ba72b
Source noteuspto-grants-2001_04