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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821992Generated: October 30, 2026

1-Bromo-3-fluorobenzene → HCID 57893715, compound

https://huagongshe.com/reaction/1821992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantSodium hydrideHCID 24758—
Reactant1-Piperidinecarboxylicacid,4-hydroxy-2-methyl-,1,1-dimethylethylester,(2S,4R)-(9CI)HCID 45097441—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 57893715HCID 5789371546%

Reaction Conditions

Temperature100 °C

Reaction Steps

Dissolve 4-hydroxy-trans-2-methyl-piperidine-1-carboxylic acid tert-butyl ester isomer 1 (preparation 2, 3.03 g, 14.07 mmol) in 1-methyl-2-pyrrolidinone (50 mL), treat with 95% sodium hydride (0.33 g, 12.93 mmol), stir and beat at 70° C. After 1 hr., add 1-bromo-3-fluoro-benzene (1.73 mL, 15.5 mmol), stir, and heat at 100° C. After 16 hr., cool to ambient temperature and quench with water (100 mL). Extract with 4:1 hexane:ethyl acetate (2×100 mL), combine the organic layers and wash with aqueous NaCl solution (75 mL), dry over sodium sulfate, filter and concentrate. Purify the residue by silica gel flash chromatography eluting with 4:1 hexanes:ethyl acetate to obtain of the title compound (2.42 g, 46%). 1H NMR (CDCl3): 7.1 (m, 3H), 6.8 (m, 1H), 4.55 (m, 1H), 4.5 (m, 1H), 4.1 (m, 1H), 2.95 (m, 1H), 2.1 (m, 1H), 1.95 (m, 1H), 1.7 (m, 1H), 1.5 (m, 1H), 1.45 (s, 9H), 1.2 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608629B2
Source datasetuspto-grants-2009_10
ORD IDord-d694c2ccbfe04f5db5b8dc16d338c51e
Source noteuspto-grants-2009_10