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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005129Generated: October 30, 2026

Benzyl Bromide → HCID 86755336, compound

https://huagongshe.com/reaction/1005129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 86755337HCID 86755337—
ProductHCID 86755336HCID 86755336—

Reaction Steps

(ddd) In an analogous manner to that described in Example 1 (g), by alkylating tert-butyl (3SR,4RS,5RS)-4-(4-hydroxymethyl-phenyl)-3-methoxymethyl-5-(naphthalen-2-yl-methoxy)-piperidine-1-carboxylate with benzyl bromide there was obtained tert-butyl (3SR,4RS,5RS)-4-(4-benzyloxymethyl-phenyl)-3-methoxymethyl-5-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate as a colourless oil; MS: 582 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-b11b065ddcf4454f9e639eda8e0c9573
Source noteuspto-grants-2000_04