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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870073Generated: October 30, 2026

Hydrochloric Acid → (E)-N-Hydroxy-3-[(toluene-4-sulfonyl)-1-H-pyrrol-3-yl]-acrylamide

https://huagongshe.com/reaction/870073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantO-(Trimethylsilyl)hydroxylamineHCID 2734666—
Reactant(E)-3-[1-(toluene-4-sulfonyl)-1H-pyrrol-3-yl]-acrylic acidHCID 66646287—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-N-Hydroxy-3-[(toluene-4-sulfonyl)-1-H-pyrrol-3-yl]-acrylamideHCID 1168809920.6%

Reaction Steps

0.231 g of (E)-3-[1-(toluene-4-sulfonyl)-1H-pyrrol-3-yl]-acrylic acid (compound A1) are dissolved in 8 ml of dichloromethane at room temperature. Then 50 μl of N,N-dimethylformamide (DMF) are added, 0.275 g of oxalic acid chloride dissolved in 2 ml of dichoromethane are added dropwise and stirred for 1.5 hour. To the solution are added 0.439 g of O-(trimethylsilyl)hydroxylamine and stirred for 15 minutes. Then 20 ml of aqueous hydrochloric acid (1 M strength) are added and extracted with ethyl acetate. The combined organic phase is dried over sodium sulfate. Afterwards it is filtered and evaporated under vacuo. The crude product is purified by silica gel flash chromatography using a gradient of dichloromethane and methanol from 98:2 to 6:4 to yield 0.050 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969401B2
Source datasetuspto-grants-2015_03
ORD IDord-2152304e404a45b196e57a24e2d236bf
Source noteuspto-grants-2015_03