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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657672Generated: October 30, 2026

Oxalic Acid → HCID 178461428, compound

https://huagongshe.com/reaction/657672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantOxalateHCID 71081—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57672031HCID 57672031—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 178461428HCID 17846142819.3%

Reaction Steps

A To a solution of (3S)-1-{3-[4-(4-oxocyclohexyl)phenoxy]propyl}-3-methylpiperidine (170 mg) in methanol (5 mL) is added sodium borohydride (20 mg). The mixture is stirred for one hour at room temperature, and then concentrated under reduced pressure. The residue is partitioned between water (5 mL) and ethyl acetate (10 mL). The aqueous phase is extracted twice with ethyl acetate. The organic extracts are pooled, dried over magnesium sulfate, concentrated under reduced pressure to give 129 mg of crude base which is converted to the oxalate with oxalic acid (35 mg) in a mixture of ethanol and diethyl ether, giving 33 mg of (3S)-1-{3-[trans-4-(4-hydroxycyclohexyl)phenoxy]propyl}-3-methylpiperidine, oxalate as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076329B2
Source datasetuspto-grants-2011_12
ORD IDord-fbb6f5136c484dbf80c1a0b3f5511541
Source noteuspto-grants-2011_12