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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571801Generated: October 30, 2026

Ammonium Hydroxide → HCID 66656124, compound

https://huagongshe.com/reaction/571801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 66653900HCID 66653900—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 66656124HCID 66656124—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-{2-[4-(2-Chloro-phenoxy)-phenyl]-thiomorpholin-4-yl}-propionic acid tert-butyl ester (0.28 g; 0.65 mmol) in MeOH (10 mL) was added, dropwise, a solution of OXONE® (0.20 g; 0.32 mmol) in water (10 mL), at 0° C. The mixture was stirred for 2 hours at 0° C., and then allowed to warm to room temperature overnight. Subsequently, water, brine, and 25% aqueous NH4OH were added and the mixture extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, CH2Cl2/MeOH 98:2) to afford 3-{2-[4-(2-Chloro-phenoxy)-phenyl]-1-oxo-thiomorpholin-4-yl}-propionic acid tert-butyl ester (0.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029371B2
Source datasetuspto-grants-2015_05
ORD IDord-7960b30b30114715afa3d9c706477afb
Source noteuspto-grants-2015_05