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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272621Generated: October 30, 2026

Nitromethane → HCID 86729779, compound

https://huagongshe.com/reaction/2272621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86729778HCID 86729778—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 86729779HCID 8672977977%

Reaction Steps

The compound obtained in Step 1 (21.69 g, 98.31 mmol), DBU (16.30 mL, 108.14 mmol) and nitromethane (6.00 g, 98.31 mmol) were stirred at room temperature for 14 hr. To the reaction solution was added brine at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5 to 30% ethyl acetate/hexane) to give N-(3-chloro-4-cyanophenyl)-3-methyl-4-nitrobutanamide (21.20 g, 75 mmol, 77%) as a pale-orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-40f94f87774c4ff2b8f30007eaeb83dd
Source noteuspto-grants-2015_09