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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Piperidinecarboxylicacid,4-hydroxy-2-methyl-,1,1-dimethylethylester,(2S,4R)-(9CI) | HCID 45097441 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 57893715 | HCID 57893715 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608629B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-d694c2ccbfe04f5db5b8dc16d338c51e |
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| Source note | uspto-grants-2009_10 |
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