HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl alcohol → Benzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl alcohol | HCID 72850 | — |
| Reactant | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178478041 | HCID 178478041 | — |
| Product | Benzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylate | HCID 23157061 | — |
Reaction Steps
9.74 g of the entitled compound was obtained as a pale yellow oily substance in the same manner as in Production Example 8-3, for which, however, benzyl 4-oxopiperidine-1-carboxylate was used in place of tert-butyl 3-oxo-8-aza-bicyclo-[3.2.1]octane-8-carboxylate used in Production Example 8-3, and 2-chlorophenylmagnesium bromide was used in place of the lithium reagent prepared from 2-bromobenzyl alcohol and n-butyllithium.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855294B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-1950dbe6c9334b188344b4d0d6084a4f |
| Source note | uspto-grants-2010_12 |