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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963597Generated: October 29, 2026

Ethanol heptane → (2S,4R)-Methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1963597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol heptaneHCID 22502148—
Reactant(2R,4S)-Methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylateHCID 68506974—
SolventAcetonitrileHCID 6342—
Product(2S,4R)-Methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylateHCID 6673515087.4%
Product(2R,4S)-Methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylateHCID 68506974—

Reaction Steps

Cis-methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylate (1.36 g, 3.87 mmol) was subjected to chiral preparative HPLC (Column: Chiralpak AD (250×20), 5 μm particle size, mobile phase: Heptane/EtOH/FA 90/10/0.2, flow rate 18 mL/min) to yield (2R,4S)-methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylate (550 mg (40%), Chiral purity 98.2% ee, Optical rotation [α]D20=+15.0 (acetonitrile, c=1) and (2S,4R)-methyl 2-(3,4-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylate (596 mg, 44%), Chiral purity 99.4% ee, Optical rotation [α]D20=−13.2 (acetonitrile, c=1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-6f7c5fc9542b42f88d5cfacd08c07196
Source noteuspto-grants-2013_04