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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432891Generated: November 1, 2026

Acetylglycine → HCID 54316039, compound

https://huagongshe.com/reaction/1432891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylglycineHCID 10972—
Reactant2-Thiophenecarboxaldehyde, 5-chloro-HCID 81700—
ReactantSodium AcetateHCID 517045—
SolventDichloromethaneHCID 6344—
SolventAcetic AnhydrideHCID 7918—
SolventSodium HydroxideHCID 14798—
ProductHCID 54316039HCID 54316039100%

Reaction Steps

A mixture consisting of 5-chlorothiophene-2-carboxaldehyde (1.00 g, 6.82 mmol), N-acetylglycine (0.96 g, 8.18 mmol), NaOAc (0.67 g, 8.18 mmol) in Ac2O (5 mL) is warmed at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and diluted with dilute aqueous NaOH (0.5 M, 100 mL) and CH2Cl2 (100 mL). The layers are separated and the organic phase is washed with aqueous NaHCO3, brine, dried over anhydrous Na2SO4, filtered and concentrated to provide 1.5 g (100%) of the title compound as a colorless oil which is used without further purification in the next reaction. 1H NMR (300 MHz, CDCl3) δ2.39 (s, 3H), 6.94 (d, J=4.0 Hz, 1H), 7.21 (s, 1H), 7.26 (d, J=4.0 Hz, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-da6c9100ec0446b181cb1583437fc61e
Source noteuspto-grants-2009_11