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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921260Generated: October 31, 2026

Dimethylformamide → (3-Chloro-2-nitrophenyl)(m-tolyl)methanone

https://huagongshe.com/reaction/921260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant3-Chloro-2-nitrobenzoic acidHCID 20902—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178425413HCID 178425413—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloro-2-nitrophenyl)(m-tolyl)methanoneHCID 86713380—

Reaction Steps

A solution of 3-chloro-2-nitrobenzoic acid (2.5 g, 12.40 mmol) in tetrahydrofuran (50 mL) was treated with oxalyl chloride (1.194 mL, 13.64 mmol) followed by DMF (0.096 mL, 1.240 mmol). The reaction mixture was stirred at room temperature for 2 hrs. After cooling to 0° C., a 1M solution of m-tolylmagnesium bromide (24.81 mL, 24.81 mmol) was added. After 1 hr another portion of m-tolylmagnesium bromide (24.81 mL, 24.81 mmol) was added. After 1 hour, the reaction mixture was partitioned between ethyl acetate (200 mL) and 1N HCl (150 mL). The aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic phases were dried over Na2SO4, filtered and concentrated. The crude material was purified by flash chromatography (Teledyne ISCO CombiFlash Rf, 0% to 100% solvent A/B=ethyl acetate/heptane, REDISEP® SiO2 120 g) to provided Intermediate A-18A (0.700 g, 21%). 1H NMR (400 MHz, DMSO-d6) δ 8.04 (dd, J=8.1, 1.1 Hz, 1H), 7.82 (t, J=7.9 Hz, 1H), 7.71 (dd, J=7.7, 1.1 Hz, 1H), 7.66-7.54 (m, 3H), 7.52-7.46 (m, 1H), 2.40 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273014B2
Source datasetuspto-grants-2016_03
ORD IDord-02affd7d6610405f80acbe71a98d3515
Source noteuspto-grants-2016_03