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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514812Generated: October 30, 2026

Iodine → HCID 22975820, compound

https://huagongshe.com/reaction/514812

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 acetate/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 numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-33f31bd005614aaf841135b4a0ebda3a
Source noteuspto-grants-2015_08