Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377925Generated: October 31, 2026

Sodium Carbonate → HCID 22915473, compound

https://huagongshe.com/reaction/1377925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantO-tert-butylhydroxylamine hydrochlorideHCID 2777906—
ReactantHCID 12412295HCID 12412295—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventThionyl ChlorideHCID 24386—
ProductHCID 22915473HCID 2291547398%

Reaction Steps

A suspension of 3-(4-iodophenoxy)propanoic acid (1.00 g, 3.42 mmol) in thionyl chloride (6.0 mL) was heated at reflux for 30 minutes. The reaction mixture was cooled to ambient temperature, diluted with ethyl ether, and concentrated in vacuo. The residue was azeotroped three times with ethyl ether, dried under high vacuum, and taken up in dichloromethane (7 mL) under N2. To the solution was added a solution in dichloromethane of O-tert-butylhydroxylamine (8.60 mmol; prepared by dissolving O-tert-butylhydroxylamine hydrochloride in water, making the free base with aqueous 10% Na2CO3, and extracting the solution with dichloromethane, and drying the organic solution over MgSO4), and the reaction mixture was stirred for two hours. The reaction mixture was washed with saturated aqueous NaHCO3 and brine, dried over Na2SO4, filtered, and concentrated in vacuo to give a yellow oil which crystallized on standing to give O-tert-butyl 3-(4-iodophenoxy)propanohydroxamic acid (1.22 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665777
Source datasetuspto-grants-1997_09
ORD IDord-9fd05fb35ff14733aaa9e82f818de036
Source noteuspto-grants-1997_09