HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016128Generated: October 31, 2026
4-Bromo-1,2-dichlorobenzene → tert-Butyl 4-(3,4-dichlorophenyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/1016128
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-1,2-dichlorobenzene | HCID 29013 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-(3,4-dichlorophenyl)-4-hydroxypiperidine-1-carboxylate | HCID 49760236 | 97.5% |
Reaction Steps
n-BuLi (2.5 M, 2 mL, 5.21 mmol) was added into a solution of 4-bromo-1,2-dichlorobenzene (1.07 g, 4.74 mmol) in dry THF (10 mL) at −78° C. The mixture was stirred for 20 mins and then a solution of tert-butyl 4-oxopiperidine-1-carboxylate (0.95 g, 4.74 mmol) in THF (5 mL) was added. The mixture was further stirred at −78° C. for 1 h. After this time, the reaction was quenched with NH4Cl (aq., 15 mL), extracted with ethyl acetate (50 mL×3), dried over Na2SO4 and concentrated to yield a residue. The residue was purified by flash chromatography using 10-30% ethyl acetate in hexanes as an eluent to provide tert-butyl 4-(3,4-dichlorophenyl)-4-hydroxypiperidine-1-carboxylate (1.6 g, 90% purity, 88% yield) as a colorless oil. MS found: 346.3 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985861B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-0c111b279ac64fc19d12d38b95f14b4c |
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| Source note | uspto-grants-2011_07 |
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