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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419352Generated: October 30, 2026

Allyl bromide → HCID 59452984, compound

https://huagongshe.com/reaction/419352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant4-Fluoro-2-iodo-1-nitrobenzeneHCID 19361948—
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178478979HCID 178478979—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59452984HCID 5945298442%

Reaction Steps

To 4-fluoro-2-iodo-1-nitrobenzene (40.0 g, 150 mmol) in THF (200 mL) at −40° C. was added phenylmagnesium chloride (80.0 mL, 2M in THF, 161 mmol) dropwise. The reaction was stirred for 30 min followed by dropwise addition of CuCN.2LiCl (26.0 g, 150 mmol) in THF. The mixture was stirred an additional 30 min at which time allyl bromide (20.0 g, 161 mmol) was added. The reaction was stirred at −40° C. for 2 h followed by rt overnight. The reaction was quenched with saturated ammonium chloride and extracted with EtOAc. The organic layer was washed with brine, dried (MgSO4) and concentrated. Purification by flash chromatography provided the title compound of step B (11.0 g, 60.7 mmol, 42%). 1H NMR (400 MHz, CDCl3) δ ppm 3.70 (d, J=6.4 Hz, 2H), 5.08-5.71 (m, 2H), 6.87-6.02 (m, 1H), 7.01-7.11 (m, 2H), 7.95-8.05 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-ba674dbad0a6445ca01fdd551ac43752
Source noteuspto-grants-2012_01