HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258875Generated: November 1, 2026
Methyl iodide → 4-(4-Fluoro-phenyl)-1-methyl-1H-[1,2,3]triazole
https://huagongshe.com/reaction/1258875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-Ethynyl-4-fluorobenzene | HCID 522627 | — |
| Reactant | sodium L-ascorbic acid | HCID 66586226 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Fluoro-phenyl)-1-methyl-1H-[1,2,3]triazole | HCID 67495571 | 286.4% |
Reaction Steps
The reaction mixture was splitted in 24 tubes of 1.00 g (8.32 mmol) each. A mixture of 1-ethynyl-4-fluorobenzene (24.0 g, 200 mmol), sodium azide (14.41 g, 222 mmol), iodomethane (14.93 mL, 240 mmol), copper(I) iodide (8.03 g, 42 mmol) and L-(+)-ascorbic acid sodium salt (7.84 g, 40 mmol) in water (240 mL) was heated at 75° C. for 10 h. The mixture was then diluted with dichloromethane (25 mL) and filtered off. The aqueous layer of the filtrate was extracted with dichloromethane and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 5% methanol in dichloromethane) afforded the title compound (20.3 g, 57%) as a white solid after recrystallisation from ethyl acetate-heptane. MS: m/e=178.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466181B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-1d974565c289454c935064bc6155bee9 |
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| Source note | uspto-grants-2013_06 |
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