HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969124Generated: October 30, 2026
tert-Butyl 4-oxopiperidine-1-carboxylate → 1-(4-[1-(Tert-butoxycarbonyl)-4-hydroxypiperidin-4-yl]phenyl}cyclopropanecarboxylic acid
https://huagongshe.com/reaction/969124
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | 1-(4-Bromophenyl)cyclopropane-1-carboxylic acid | HCID 16227966 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178448196 | HCID 178448196 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1-(4-[1-(Tert-butoxycarbonyl)-4-hydroxypiperidin-4-yl]phenyl}cyclopropanecarboxylic acid | HCID 66661592 | — |
Reaction Steps
A solution of 1-(4-bromophenyl)cyclopropanecarboxylic acid (1000.0 mg, 0.0041480 mol) in tetrahydrofuran (30 mL, 0.4 mol) was cooled below −20° C. under a N2 atmosphere and dibutylmagnesium in heptane (1.0 M, 2.2 mL) was slowly added to the solution while the reaction temperature was maintained below −20° C. Then 2.5 M of n-butyllithium in hexane (1.8 mL) was slowly added to the mixture below −20° C. under effective stirring. After stirring below −20° C. for 1 h, a solution of tert-butyl 4-oxo-1-piperidinecarboxylate (0.909 g, 0.00456 mol) in THF (20.0 mL) was added to the mixture below −20° C. After stirring below −20° C. for 1 h, the reaction was quenched with ammonium chloride. The product was extracted with EtOAc and the combined extract was washed with brine, dried over Na2SO4, and filtered. The filtrate was concentrated and then purified by Combiflash, eluting with 5% methanol in methylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304081B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-e1d2cfed3d6b4fd29a5995317846153f |
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| Source note | uspto-grants-2007_12 |
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