HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → Ethyl 4-(3-bromopropyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Tert-butyl 4-ethyl 4-(3-hydroxypropyl)piperidine-1,4-dicarboxylate | HCID 57815239 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(3-bromopropyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate | HCID 67539218 | — |
Reaction Steps
Carbon tetrabromide (1.6 gm, 0.0048 mol) is added to a stirred solution of 4-(3-hydroxypropyl) piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester (1.27 gm, 0.0040 mol) and triphenyl phosphine (1.6 gm, 0.0060 mol) in dichloromethane (15 mL) at 0-5° C. temperature. Reaction mixture is allowed to stir at room temperature for 30 minutes. Removal of solvent gives a crude residue which is purified by column chromatography (silica gel 230-400 mesh, ethyl acetate:n-hexane 3:7) to get 4-(3-bromopropyl)piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266867B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-70e5d75e610f49728e35a6b0da7832f8 |
| Source note | uspto-grants-2016_02 |