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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279174Generated: October 30, 2026

Ammonium Chloride → HCID 10264208, compound

https://huagongshe.com/reaction/279174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
ReactantMagnesiumHCID 5462224—
ReactantHCID 14978394HCID 14978394—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10264208HCID 10264208103.6%

Reaction Steps

1-Bromo-2-fluorobenzene (15 g) and 4-[(2S)-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propionyl]morpholine (40 g) were dissolved in tetrahydrofuran (200 ml), to which magnesium (turnings: 4.4 g) was added. The mixture was stirred vigorously. The reaction flask was cooled when the temperature of the reaction solution reached to 35° C., and 1-bromo-2-fluorobenzene (16.7 g) was added thereto over the period of 10 minutes while the temperature of the reaction solution was kept at 35 to 37° C. After the reaction solution was stirred at 30 to 35° C. for 2 hours, it was cooled in an icebath. A saturated aqueous solution of ammonium chloride (100 ml) was added thereto and the mixture was extracted with ethyl acetate (200 ml×2,100 ml). The extract was washed with water and a saturated aqueous solution of sodium chloride successively, dried over anhydrous magnesium sulfate, and distilled under reduced pressure to remove the solvent. The residue was subjected to silica gel chromatography (eluent: hexane/ethyl acetate=10/1 to 5/1) to give (2S)-2′-fluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)-propiophenone (22.4 g) as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362206B1
Source datasetuspto-grants-2002_03
ORD IDord-355bb9b9a3134f3d85e074b8d9ace153
Source noteuspto-grants-2002_03