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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265148Generated: October 27, 2026

2-Bromobenzyl alcohol → Benzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2265148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl alcoholHCID 72850—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178478041HCID 178478041—
ProductBenzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855294B2
Source datasetuspto-grants-2010_12
ORD IDord-1950dbe6c9334b188344b4d0d6084a4f
Source noteuspto-grants-2010_12