HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542790Generated: November 1, 2026
Thionyl Chloride → N-(1-methoxy-2,2,2-trichloroethyl)nicotinamide
https://huagongshe.com/reaction/542790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-(2,2,2-trichloro-1-hydroxyethyl)nicotinamide | HCID 246390 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(1,2,2,2-tetrachloroethyl)nicotinamide | HCID 20207309 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(1-methoxy-2,2,2-trichloroethyl)nicotinamide | HCID 13671519 | — |
Reaction Steps
150 ml of benzene was added to 10.0 g of N-(1-hydroxy-2,2,2-trichloroethyl)nicotinamide. 5.3 g of thionyl chloride was added dropwise thereto and the mixture was heated under reflux (60° to 80° C.) for about 5 h under stirring to complete the production of N-(1,2,2,2-tetrachloroethyl)nicotinamide. The reaction liquid was cooled to 30° C. or below. 20 ml of methanol was added to the liquid. 4.0 g of triethylamine was added dropwise to the liquid mixture while it was kept at 5° C. and the obtained mixture was stirred at room temperature for 3 h. Then, the mixture was kept at room temperature overnight. The reaction liquid was poured in an aqueous sodium bicarbonate solution and a benzene layer thus separated was washed with saturated aqueous common salt solution and water and dried over anhydrous sodium sulfate. After concentration, the residue was recrystallized from methanol to obtain 4.8 g of N-(1-methoxy-2,2,2-trichloroethyl)nicotinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659722 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-b386df8ab5ad45a9b76eb7c868224d34 |
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| Source note | uspto-grants-1987_04 |
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