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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553465Generated: October 26, 2026

Hydrochloric Acid → 2-(Tert-butylsulfamoyl)acetic acid

https://huagongshe.com/reaction/553465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantethyl-2-(N-tert-butylsulfamoyl)acetateHCID 19833529—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(Tert-butylsulfamoyl)acetic acidHCID 2877341669%

Reaction Steps

To a solution of ethyl-2-(N-tert-butylsulfamoyl)acetate (4 g, 17.9 mmol.) in 65 mL of EtOH and 13 mL of H2O at 0° C. was slowly added NaOH (3.6 g, 89.5 mmol.). The reaction was allowed to room temperature and stirred overnight. TLC analysis showed the reaction complete. The mixture was acidified to pH=5 with aq. HCl (1M). The resulting mixture was extracted with EtOAc (30 mL×3). The combined organic layer was dried over Na2SO4, concentrated to afford crude 2-(N-tert-butylsulfamoyl)acetic acid (2.4 g, 69%), which was used directly without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048862B2
Source datasetuspto-grants-2011_11
ORD IDord-2407a5ae7760488f90a884c11ea4060b
Source noteuspto-grants-2011_11