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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502024Generated: November 2, 2026

2-Chloro-N-methoxy-N-methylacetamide → HCID 86727073, compound

https://huagongshe.com/reaction/1502024

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N-methoxy-N-methylacetamideHCID 2734716—
Reactant3-Iodo-2-methylbenzonitrileHCID 23091876—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86727073HCID 86727073—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-iodo-2-methylbenzonitrile (7.71 g, 31.7 mmol) and 2-chloro-N-methoxy-N-methylacetamide (6.55 g, 47.6 mmol) in THF (100 mL) at −78° C. was added n-butyllithium (2.5 M in hexanes, 14.0 mL, 34.9 mmol) dropwise. After complete addition, the mixture was stirred 15 min. at −78° C., then quenched with the dropwise addition of 1 N HCl. The mixture was partitioned between EtOAc/water and the layers separated. The aqueous was extracted with EtOAc (2×) and the combined organic layers were washed with brine, dried (magnesium sulfate), filtered and concentrated. Recrystallization of the resulting residue from hexanes provided 3-(2-chloroacetyl)-2-methylbenzonitrile: 1H NMR (500 MHz, CDCl3), δ 7.76 (m, 2H), 7.41 (m, 1H), 4.55 (s, 2H), 2.68 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-f6caecd7f0f44a09bede8eb23c8ed3b9
Source noteuspto-grants-2015_12