HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858578Generated: November 4, 2026
HCID 54062527, compound → HCID 22128508, compound
https://huagongshe.com/reaction/1858578
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 54062527 | HCID 54062527 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22128508 | HCID 22128508 | 101.7% |
Reaction Steps
A solution of 280 mg (0.63 mmol) of tert-butyl (3RS,4RS)-3-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethoxy)-4-(4-fluorophenyl)-piperidine-1-carboxylate in 5 ml of dry methylene chloride was treated with 808 mg (1.89 mmol) of anhydrous zinc bromide and the mixture was stirred at room temperature for 5 hours. Subsequently, the solvent was distilled off under reduced pressure, the residue was taken up in 10 ml of methanol, treated with 2 ml of 2N sodium hydroxide solution and the solid was separated. The filtrate was evaporated under reduced pressure and the residue was partitioned between methylene chloride and water. The organic phase was separated and evaporated under reduced pressure. There were obtained 220 mg (98% of theory) of (3RS,4RS)-3-(2,3-dihydrobenzo[1,4]dioxin-6-yl-methoxy)-4-(4-fluorophenyl)-piperidine as a yellowish solid; MS: 344 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150526 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-a041aa7b316e4b2a8c6499e5878704f9 |
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| Source note | uspto-grants-2000_11 |
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