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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920577Generated: October 30, 2026

Sodium Hydroxide → HCID 67031880, compound

https://huagongshe.com/reaction/920577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
ReactantHCID 86670014HCID 86670014—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67031880HCID 6703188048.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3-[2-(4-Acetylsulfanyl-phenyl)-morpholin-4-yl]-propionic acid tert-butyl ester (0.31 g; 0.85 mmol) and NaOH (37 mg, 0.93 mmol) in EtOH (10 mL) and water (1 mL) was stirred for 30 min at 0° C. Subsequently, 2,6-dichlorobenzyl bromide (0.22 g; 0.93 mmol), dissolved in EtOH (2.5 mL), was added, and the mixture allowed to warm to RT. After 90 min. the mixture was partitioned between EtOAc and 5% aqueous NaHCO3. The layers were separated, and the organic layer was washed with 5% aqueous NaHCO3 and brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, CH2Cl2/acetone 95:5) to afford 3-{2-[4-(2,6-dichloro-benzylsulfanyl)-phenyl]-morpholin-4-yl}-propionic acid tert-butyl ester (0.20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-44bbf08465924325bf5bb305b2056a6d
Source noteuspto-grants-2016_03