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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588257Generated: October 30, 2026

Ammonium Hydroxide → HCID 66656124, compound

https://huagongshe.com/reaction/588257

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 numberUS09227960B2
Source datasetuspto-grants-2016_01
ORD IDord-7425bb4c659d4d04be66f40d13d9d176
Source noteuspto-grants-2016_01