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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432051Generated: November 1, 2026

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

https://huagongshe.com/reaction/1432051

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

To a stirred solution of 4-amino-3-chloro-5-methylbenzonitrile (0.516 g, 3.1 mmol) in 10 mL of THF at room temperature was added 6.6 mL of 1.0 M NaHMDS in THF. The resulting reaction mixture was stirred at room temperature for 30 min., at which time acetyl chloride (3.1 mmol) was added. DCM (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 DCM (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 numberUS07612069B2
Source datasetuspto-grants-2009_11
ORD IDord-a338b5ea49fc42958d79925c13d421b3
Source noteuspto-grants-2009_11