HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249884Generated: October 30, 2026
Dibromodifluoromethane → HCID 11608680, compound
https://huagongshe.com/reaction/2249884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromodifluoromethane | HCID 6382 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11608680 | HCID 11608680 | 56% |
Reaction Steps
To a solution of 4-oxo-piperidine-1-carboxylic acid benzyl ester (0.50 g, 2.14 mmol, 1.0 eq.) in THF (20 mL) was added dibromodifluoromethane (0.90 mL, 4.5 eq.) at −30° C. followed by HMPA (1.75 mL, 4.5 eq.). The cooling bath was removed and the reaction mixture was swirled periodically. After 30 min, zinc dust (0.63 g, 4.5 eq.) and HMPA (80 μL 0.4 eq.) was added and the mixture was heated at reflux for 18 h. Upon cooling to room temperature, the residue was washed with diethyl ether several times. The combined ether washings were washed successively with saturated aqueous copper (II) sulphate, brine, dried over Na2SO4 and concentrated. The residue was purification by chromatography (20% EtOAc-hexanes) to afford 4-difluoromethylene-piperidine-1-carboxylic acid benzyl ester (0.32 g, 56%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314936B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-34b0c99d40814169ac17e2f972e485b3 |
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| Source note | uspto-grants-2008_01 |
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