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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 3-Methyl-2-thenoic acid | HCID 90269 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene ethylacetate | HCID 21584019 | — |
| Product | Nitromethyl 3-methyl-2-thienyl ketone | HCID 18541419 | 19.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932765 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-2f67b0a9ffa94a979ffc1339ed168dfc |
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| Source note | uspto-grants-1999_08 |
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