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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524405Generated: October 30, 2026

N-chlorosuccinamide → HCID 86669542, compound

https://huagongshe.com/reaction/524405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-chlorosuccinamideHCID 15238416—
Reactant76687-08-6HCID 83668651—
SolventAcetonitrileHCID 6342—
ProductHCID 86669542HCID 8666954286.2%

Reaction Steps

2-(2-Amino-thiazol-4-yl)-2-methyl-propionic acid ethyl ester (0.3 g, 1.40 mmol) was taken in 10 mL of acetonitrile and N-Chlorosuccinamide (0.224 g, 1.68 mmol) was added the reaction was stirred for 1 hr. at room temperature. After completion of reaction acetonitrile was evaporated under reduced pressure and the residue was partitioned between water (25 mL) and ethyl acetate (25 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×25 mL). The combined organic layer was washed with brine and dried over anhydrous sodium sulphate and the solvent was removed in vacuo. The residue was purified by preparative TLC plate (mobile phase 40% ethyl acetate in hexane) to afford pure compound (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-718b0b7b56904ee99f0657950fe86525
Source noteuspto-grants-2016_05