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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366476Generated: October 30, 2026

1-Bromo-2-fluoro-4-iodobenzene → HCID 58938107, compound

https://huagongshe.com/reaction/2366476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-fluoro-4-iodobenzeneHCID 2725006—
Reactanttert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58938107HCID 5893810774.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-bromo-2-fluoro-4-iodobenzene (44.22 g, 0.147 mol) in tetrahydrofuran (160 mL) was added isopropylmagnesium chloride (2.0 M solution in tetrahydrofuran, 73.5 mL) at 0° C. and the mixture stirred at 0° C. for 3 hours. This solution was cannulated into a solution of 1-BOC-2-piperidone (24.4 g, 0.122 mol) in tetrahydrofuran (240 mL) at −78° C. and the mixture stirred at −78° C. for 1 hour. The solution was warmed to ambient temperature and stirred for one hour before quenching with water. Hydrochloric acid (2N, 120 mL) was added and the mixture stirred at ambient temperature for 10 minutes. The mixture was concentrated and the residue partitioned between ethyl acetate and brine. The organic layer was washed with brine, dried over magnesium sulfate and filtered. Concentration afforded the crude product which was recrystallized from hexane and dichloromethane to give 33.95 g of the title compound as a white solid. 1HNMR (CDCl3) δ 1.44 (s, 9H), 1.52-1.63 (m, 2H), 1.70-1.83 (m, 2H), 2.96 (t, J=7.1 Hz, 2H), 3.16 (q, J=6.4 Hz, 2H), 4.58 (s, 1H), 7.59-7.71 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697736B2
Source datasetuspto-grants-2014_04
ORD IDord-89c5f9a1241a41beafabd8b986714c2c
Source noteuspto-grants-2014_04