Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720610Generated: November 2, 2026

4-Methoxybenzenesulfonyl chloride → HCID 3113410, compound

https://huagongshe.com/reaction/1720610

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 3113410HCID 3113410—

Reaction Conditions

Temperature0 °C

Reaction Steps

Glycine ethyl ester hydrochloride (31.39 g, 225.0 mmol) is dissolved in dioxane (150 mL) and water (150 mL), triethylamine (69.0 mL, 495.0 mmol) is added, and the solution is cooled to 0° C. To this solution is added 4-methoxybenzenesulfonyl chloride (51.15 g, 248.0 mmol) over 10 minutes. The reaction is warmed to room temperature and stirred overnight. The next day the mixture is reduced to one-half volume by evaporating solvent, diluted with 1N sodium hydroxide, and extracted well with ether. The combined organic layers are washed with brine, dried (Na2SO4), and the solvent is evaporated. The product is recrystallized from ether/ethyl acetate/hexanes to give ethyl 2-[[4-methoxybenzenesulfonyl]amino]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-d2ecd07354594a748c1e9a1c4eb79882
Source noteuspto-grants-1996_04