HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361059Generated: October 30, 2026
Imidazole → 1-Fluoro-4-((4-iodobut-2-enyloxy)methyl)-2-methylbenzene
https://huagongshe.com/reaction/1361059
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 4-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-ol | HCID 66968450 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Fluoro-4-((4-iodobut-2-enyloxy)methyl)-2-methylbenzene | HCID 66968201 | — |
Reaction Steps
To a solution of triphenylphosphine (2.6 g, 9.9 mmol) in anhydrous 40 mL DCM was added imidazole (1.4 mg, 20.4 mmol) and iodine (2.5 mg, 9.9 mmol) at 0° C. The reaction mixture was stirred for 30 min at 0° C. and then 4-(4-Fluoro-3-methylbenzyloxy)but-2-en-1-ol (1.3 g, 6.2 mmol) in 10 mL DCM was added to the mixture. The resulting mixture was stirred at 0° C. for 2 h and the temperature was slowly raised to room temp over a period of 2 h. 20 mL of 10% sodium thiosulfate was added and extracted with more DCM (3×30 mL). The combined DCM layer was washed with brine (2×30 mL) and dried over sodium sulfate. Evaporation of solvent left the crude product as an oil from which the product was isolated by Flash column chromatography eluting with 0% to 10% ethyl acetate/hexane to give the title compound, 1.5 g, as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879911B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-bc79be4db39646f3a60a62890af4a380 |
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| Source note | uspto-grants-2011_02 |
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