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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819681Generated: November 1, 2026

Hydrochloric Acid → N-(2-Chloro-4-cyano-6-methylphenyl)acetamide

https://huagongshe.com/reaction/1819681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Amino-3-chloro-5-methylbenzonitrileHCID 2735301—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-Chloro-4-cyano-6-methylphenyl)acetamideHCID 5896291034%

Reaction Steps

Step G (1). To a stirred solution of 4-amino-3-chloro-5-methylbenzonitrile (0.516 g, 3.1 mmol) in 10 mL of THF at rt was added 6.6 mL of 1.0 M NaHMDS in THF. The resulting reaction mixture was stirred at rt for 30 min., at which time acetyl chloride (3.1 mmol) was added. CH2Cl2 (100 mL) and water (100 mL) were added to the reaction mixture after being stirred overnight, followed by the addition of 5 mL of 1.4 N HCl aqueous solution. Layers were separated and the aqueous layer was extracted with CH2Cl2 (2×100 mL). The extracts were combined and solvents were evaporated in vacuo. The residue was purified by flash chromatography (5-20% EtOAc/DCM) to give 0.220 g of 4-acetamido-3-chloro-5-methylbenzonitrile. 1H NMR (500 MHz, CDCl3) δ 7.57 (s, 1 H), 7.46 (s, 1 H), 7.02 (s, 1 H), 2.31 (s, 3 H), 2.26 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601751B2
Source datasetuspto-grants-2009_10
ORD IDord-cdef897e41974f17999b50c9158c63ab
Source noteuspto-grants-2009_10