HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253999Generated: October 31, 2026
2-Bromothiophene → HCID 58179496, compound
https://huagongshe.com/reaction/253999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58179496 | HCID 58179496 | 40% |
Reaction Steps
A solution of 2-bromothiophene in THF (25 ml) was added drop wise to a suspension of Mg turnings in THF (100 mL). The mixture was stirred for 30 minutes, cooled to 0° C., and a solution of tert-butyl 4-oxopiperidine-1-carboxylate (25.0 g, 125.4 mmol) in THF (25 mL) was added dropwise. The reaction mixture was slowly warmed to RT and stirred for 1 hour until complete consumption of 2-bromothiophene was indicated by TLC. The reaction was quenched with sat. aq. NH4Cl solution (50 mL), extracted with EtOAc (200 mL), washed with H2O (50 mL) and brine solution, dried (Na2SO4), filtered, and evaporated to afford crude product as light brown oil. Purification by silica gel chromatography (25% EtOAc/hexanes) yielded tert-butyl 4-hydroxy-4-(thiophen-2-yl)piperidine-1-carboxylate (14.0 g, 40% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872031B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-72500ebfa4f146c1b98715d2103e8a87 |
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| Source note | uspto-grants-2011_01 |
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