HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412883Generated: October 28, 2026
Triphenylphosphine → 1,1-Dimethylethyl 4-[(1-methyl-1H-tetrazol-5-yl)thio]-1-piperidinecarboxylate
https://huagongshe.com/reaction/412883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | HCID 178482017 | HCID 178482017 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,1-Dimethylethyl 4-[(1-methyl-1H-tetrazol-5-yl)thio]-1-piperidinecarboxylate | HCID 18539155 | — |
Reaction Steps
To a solution of 1-tert-butoxycarbonyl-4-hydroxypiperidine (1.01 g, 5.0 mmol) in dry THF (30 mL) were added triphenylphosphine (2.0 g, 7.5 mmol) and 5-mercapto-1-methyl-1H-tetrazole (0.70 g, 6.0 mmol). To the mixture was added diisopropyl azodicarboxylate (1.2 mL, 6.0 mmol) under ice cooling, and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (100 mL), which was washed with water, saturated aqueous solution of sodium hydrogen carbonate and saturated aqueous solution of sodium chloride, successively. The solvent was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (50 g, diethyl ether-hexane 1:1) to give the titled compound as a colorless oily substance. (1.11 g, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562978B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-84cb0a1613ba4a18b48b3ac6827a6216 |
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| Source note | uspto-grants-2003_05 |
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