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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007140Generated: October 28, 2026

Pyridine → HCID 10195526, compound

https://huagongshe.com/reaction/1007140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 60110357HCID 60110357—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 10195526HCID 1019552693%

Reaction Steps

To a stirred suspension of methyl (6-nitro-3,4-dihydro-2H-1,4-benzoxazin-2-yl)acetate 2 (2.52 g, 10 mmol) and anhydrous sodium carbonate (2 g.) in anhydrous DMF (15 mL) and anhydrous pyridine (5 mL), benzoyl chloride (1.5 mL, 12.96 mmol) was added. The resulting suspension was stirred 8 hours at room temperature. The reaction mixture was then diluted with ethyl acetate (100 mL) and washed with water (3×100 mL). After separation the organic phase was dried (Na2SO4) and evaporated to dryness in vacuo to afford the title compound (3.3 g, 93%) as a yellow-orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794385B2
Source datasetuspto-grants-2004_09
ORD IDord-f2455d767ac2432ea52c77ea9eba08d1
Source noteuspto-grants-2004_09