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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005139Generated: November 2, 2026

HCID 13524712, compound → HCID 86604467, compound

https://huagongshe.com/reaction/1005139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13524712HCID 13524712—
ReactantHCID 86604468HCID 86604468—
SolventDichloromethaneHCID 6344—
ProductHCID 86604467HCID 86604467—

Reaction Steps

In an analogous manner to that described in Example 74 (f), from tert-butyl (3RS,4RS,5SR)-4-[4-(3-benzyloxy-propoxy)-phenyl]-3-hydroxymethyl-5-(2-morpholin4-yl-ethoxymethyl)-piperidine-1-carboxylate by oxidation with dimethyl sulphoxide/oxalyl chloride in methylene chloride there was obtained tert-butyl (3RS,4SR,5SR)-4-[4-(3-benzyloxy-propoxy)-phenyl]-3-formyl-5-(2-morpholin-4-yl-ethoxymethyl)-piperidine-1-carboxylate as a yellow oil; MS: 597 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-90bdd480edf9470abd974a96dfddf5e6
Source noteuspto-grants-2000_04