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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754853Generated: October 28, 2026

Ammonium Chloride → HCID 57475762, compound

https://huagongshe.com/reaction/1754853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-1-fluoro-2-iodobenzeneHCID 2782750—
Reactant2-(Allyloxy)-N-methoxy-N-methylacetamideHCID 57475761—
ReactantHCID 178418918HCID 178418918—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57475762HCID 57475762—

Reaction Steps

Scheme 1, steps C and D: To 4-bromo-1-fluoro-2-iodobenzene (0.95 equiv.) in THF (4.6 mL/g) at 0° C. is added isopropylmagnesium chloride (1.0 equiv, 20 weight percent in THF). After about 60 minutes at 0° C., a solution of 2-(allyloxy)-N-methoxy-N-methylacetamide (1.0 equiv.) (Volumes for this stage are in mL/g of this compound) in THF (2.2 mL/g) is added over about 60 minutes. The reaction mixture is quenched into a solution of NH4Cl (4.3 equiv.) in water (5.8 mL/g) at 0° C. Heptanes (7.2 mL/g) is added as the mixture is warmed to room temperature, and the layers are separated. The organic layer is washed with water (7.2 mL/g). The organic layer is concentrated while additional heptanes (4 mL/g) is added to remove water and THF. The intermediate, 2-allyloxy-1-(5-bromo-2-fluoro-phenyl)ethanone is obtained as a solution in heptanes (approximately 20-25 weight %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169271B2
Source datasetuspto-grants-2015_10
ORD IDord-afd49852250f4cdc9f4d70d26f84e543
Source noteuspto-grants-2015_10