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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373510Generated: November 1, 2026

Sodium Hydroxide → HCID 23077364, compound

https://huagongshe.com/reaction/1373510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantSodium AcetateHCID 517045—
ReactantHCID 23077361HCID 23077361—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 23077364HCID 2307736486%

Reaction Steps

In ethanol (10 ml) was dissolved 0.60 g (2 mmol) of ethyl 2-(benzyloxycarbonylamino)-2-methylpropane-1-sulfinate, and 0.9 g (2.2 mmol) of 10% aqueous sodium hydroxide solution was slowly dropped thereinto under ice-cooling. The reaction was carried out at room temperature for 1 hour and then the ethanol was distilled off. Water (10 ml), 0.18 g (2.2 mmol) of sodium acetate and 0.25 g (2.2 mmol) of hydroxylamine-O-sulfonic acid were added to the residue, and the reaction was carried out at room temperature for 1 hour. The reaction mixture was poured into water, followed by three runs of extraction with ethyl acetate. The extract solution was washed with saturated aqueous sodium hydrogencarbonate solution and then saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off and 0.49 g (yield 86%) of the thus obtained crude 2-(benzyloxycarbonylamino)-2-methylpropane-1-sulfonamide was used without further purification in the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07161032B2
Source datasetuspto-grants-2007_01
ORD IDord-229c222719b84799beed032c43d604bb
Source noteuspto-grants-2007_01