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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202348Generated: November 1, 2026

Iodine → HCID 22975820, compound

https://huagongshe.com/reaction/2202348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHomoallyl bromideHCID 21241—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 22975820HCID 2297582036.5%

Reaction Steps

To a mixture of 4-bromobut-1-ene (10.9 g, 0.08 mol) and magnesium turnings (4.8 g, 0.2 mol) in dry tetrahydrofuran (80 mL) was added a crystal of iodine and the mixture was stirred at room temperature until complete reaction had occurred. To this mixture was added tert-butyl 4-oxopiperidine-1-carboxylate (7.7 g, 0.039 mol) in tetrahydrofuran (20 mL) at 0° C. After 1 h at 0° C., and 3 h at room temperature the reaction mixture was diluted with ammonium chloride solution and extracted with ethyl acetate. After drying over Na2SO4, the solvent was removed in vacuo and the residue was purified via flash chromatography with 25% ethyl actetate/hexane to afford the title compound 16B (3.63 g) as an oil. 1H NMR (CHLOROFORM-d) δ 5.84 (d, J=6.7 Hz, 1H), 4.89-5.11 (m, 2H), 3.16 (br. s., 2H), 2.16 (d, J=9.4 Hz, 2H), 1.48-1.66 (m, 6H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365545B2
Source datasetuspto-grants-2016_06
ORD IDord-3cff3eee470b4f04ad455b5b8693605c
Source noteuspto-grants-2016_06