HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882250Generated: October 31, 2026
Triphenylphosphine → 4-((4-Chloro-2-iodophenoxy)methyl)-1-methylpiperidine
https://huagongshe.com/reaction/1882250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 1-Methyl-4-piperidinemethanol | HCID 271971 | — |
| Reactant | 4-Chloro-2-iodophenol | HCID 620234 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((4-Chloro-2-iodophenoxy)methyl)-1-methylpiperidine | HCID 58880166 | 75% |
Reaction Steps
To a stirred solution of 4-chloro-2-iodophenol (1.72 g, 6.75 mmol) in anhydrous THF (10.0 mL) were sequentially added (1-methylpiperidin-4-yl)methanol (1.31 g, 10.14 mmol) and triphenyl phosphine (2.66 g, 10.14 mmoL). The reaction mixture was cooled to 0° C., and to it diisopropyl-azodicarboxylate (1.96 mL, 10.14 mmol) was added in drop wise manner. After the addition was over, stirring continued for another 0.5 h at 0° C. and then for 12 h at room temperature. Solvents were removed in vacuum and the residue was purified by silica gel column chromatography, providing Compound 173 (1.85 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318939B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-8bc36d71bd044087a18fd16e66030a89 |
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| Source note | uspto-grants-2012_11 |
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