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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458836Generated: November 1, 2026

Ethyl bromoacetate → HCID 22097159, compound

https://huagongshe.com/reaction/1458836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantN-(2,4-Dinitronaphthalen-1-yl)-4-methylbenzene-1-sulfonamideHCID 294498—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 22097159HCID 2209715976%

Reaction Steps

60 g (155 mmol) of N-(2,4-dinitro-1-naphthyl)-4-methylphenylsulfonamide (J. Soc. Chem. 1935, 1855) were dissolved in 500 ml of anhydrous dimethylformamide under protective gas and 19.1 g (170 mmol) of potassium tert-butanolate were added a little at a time. The mixture was stirred at room temperature for about 30 minutes, and then 25.9 g (155 mmol) of ethyl bromoacetate dissolved in 50 ml of anhydrous dimethylformamide were added dropwise. The mixture was then heated at 100° C. for 90 minutes and, after cooling, poured into ice-water, and the aqueous phase was extracted with ethyl acetate. The organic phase was dried and concentrated under reduced pressure. The residue was heated with a mixture of 50 ml of toluene and 100 ml of ethanol and the resulting crystals were filtered off with suction to yield 55.7 g (76%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852017
Source datasetuspto-grants-1998_12
ORD IDord-7318bf8f18cb409fbe4953c8a561a823
Source noteuspto-grants-1998_12