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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584672Generated: October 27, 2026

Nitromethane → Nitromethyl 3-methyl-2-thienyl ketone

https://huagongshe.com/reaction/1584672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant3-Methyl-2-thenoic acidHCID 90269—
SolventDimethylformamideHCID 6228—
SolventToluene ethylacetateHCID 21584019—
ProductNitromethyl 3-methyl-2-thienyl ketoneHCID 1854141919.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution composed of 10 g (70 mmol) of 3-methyl-2-thiophenecarboxylic acid, 3.4 g (56 mmol) of nitromethane and 115 ml of DMF is cooled to 0° C. 11.9 g (72.8 mmol) of diethyl cyanophosphonate in 56 ml of DMF, and then 18.2 g (180 mmol) of triethylamine in 56 ml of DMF are added thereto successively. The medium is then stirred for 2 hours at 0° C. and for 21 hours at room temperature. The reaction medium is poured over 1 litre of a toluene/ethyl acetate (1:1) mixture, and extracted with water. This aqueous phase, acidified with 40 ml of acetic acid, is extracted with a toluene/ethyl acetate (1:1) mixture. The organic extracts are washed with water and then with a saturated NaCl solution in water, before being dried over Na2SO4 and concentrated. The residue, purified by chromatography on a silica column in dichloromethane and then by recrystallization from an ethyl acetate-hexane mixture, gives 2 g of a pale yellow solid (Yield=19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932765
Source datasetuspto-grants-1999_08
ORD IDord-2f67b0a9ffa94a979ffc1339ed168dfc
Source noteuspto-grants-1999_08