HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384979Generated: October 31, 2026
Triphenylphosphine → 3-(4-Bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidine
https://huagongshe.com/reaction/1384979
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Bromo-2,6-dimethylphenol | HCID 16919 | — |
| Reactant | (1-Methyl-3-piperidyl)methanol | HCID 97998 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidine | HCID 9948656 | 66.2% |
Reaction Steps
3-Hydroxymethyl-1-methylpiperidine (0.4 mL, 3.14 mmol) and triphenylphosphine (1.01 g, 3.85 mmol) were added to a solution of 4-bromo-2,6-dimethylphenol (517 mg, 2.57 mmol) in tetrahydrofuran (10 mL) at 0° C. under dry nitrogen, followed by the dropwise addition of diethyl azodicarboxylate (0.57 mL, 3.60 mmol). The mixture was stirred at 0° C. for 4 hours and the solvent removed in vacuo. The residue was purified on silica gel, eluting with 5% methanol in dichloromethane containing 0.25% ammonium hydroxide, to give 3-(4-bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidine as an oil (531 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262078B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-398eaab2aa0c4960b356c18f8627fb95 |
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| Source note | uspto-grants-2001_07 |
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