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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821993Generated: November 2, 2026

1-Bromo-3-fluorobenzene → HCID 57893670, compound

https://huagongshe.com/reaction/1821993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantSodium hydrideHCID 24758—
Reactantcis-1-Benzyl-3-methylpiperidin-4-olHCID 57893755—
SolventDimethylformamideHCID 6228—
ProductHCID 57893670HCID 57893670—

Reaction Conditions

Temperature80 °C

Reaction Steps

Dissolve 1-benzyl-cis-3-methyl-piperidin-4-ol (preparation 6, 3.84 g, 18.73 mmol) in dry N,N-dimethylformamide (100 mL), treat with 60% sodium hydride (1.05 g, 26.22 mmol), heat and stir at 80° C. After 1 hr., add-1-bromo-3-fluoro-benzene (2.51 mL, 22.45 mmol), stir and heat at 110° C. After 16 hr., cool to ambient temperature. Partition between water (100 mL) and ethyl acetate (100 mL), wash the aqueous layer with ethyl acetate (2×100 mL), combine the organic layers, wash with water (5×100 mL) and aqueous NaCl solution (100 mL). Dry the organic layer over sodium sulfate, filter and concentrate. Purify the residue by silica gel flash chromatography eluting with 2% (2M NH3/methanol)/methylene dichloride to obtain the title compound as a mixture of enantiomers (1.69 g, 24%). 1H NMR (CDCl3): 7.3 (m, 5H), 7.1 (m, 3H), 6.8 (m, 1H), 4.3 (m, 1H), 3.5 (d, 2H), 2.5 (m, 2H), 2.4 (m, 2H), 2.0 (m, 2H), 1.8 (m, 1H), 1.0 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608629B2
Source datasetuspto-grants-2009_10
ORD IDord-f100d98cfb044d30bd580fbf503b7211
Source noteuspto-grants-2009_10