HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromodiphenyl Ether → HCID 22600006, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromodiphenyl Ether | HCID 7565 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | HCID 178419636 | HCID 178419636 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22600006 | HCID 22600006 | 45% |
Reaction Steps
To an 100 ml tetrahydrofuran solution of 3.5 g of N-tert-butoxycarbonyl-4-piperidone, a 35 ml of 4-phenoxyphenyl magnesium bromide prepared from 4-bromodiphenyl ether (0.6 mol/l tetrahydrofuran solution) was dropwise added under ice cooling and the resultant mixture was stirred for 1 hour. To the reaction mixture was added a 30 ml of saturated aqueous ammonium chloride solution. The product was extracted with ether. The extract was washed with saturated saline, dried, filtered, then concentrated under reduced pressure to give a residue, which was then purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to give N-tert-butoxycarbonyl-4-(4-phenoxyphenyl)-4-piperidinol in an amount of 2.92 g (yield 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525199B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-5500bcd7baae4c94beac6f65950f71d9 |
| Source note | uspto-grants-2003_02 |