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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528293Generated: October 31, 2026

HCID 68079399, compound → HCID 66850120, compound

https://huagongshe.com/reaction/1528293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68079399HCID 68079399—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 66850120HCID 6685012096%

Reaction Steps

Pearlman's catalyst (0.24 g) was added to an EtOH (25 ml) solution of (4aS,8aR) -tert-butyl 4-benzyldecahydroquinoxaline-1-carboxylate (2.4 g, 7.26 mmol). This suspension was stirred at room temperature for 1 hour in a hydrogen atmosphere. The catalyst was filtered through celite, and the residue was washed with EtOH. Then, the filtrate was concentrated under reduced pressure to obtain (4aS,8aR)-tert-butyl decahydroquinoxaline-1-carboxylate (1.67 g, yield: 96%) in a colorless oil form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090572B2
Source datasetuspto-grants-2015_07
ORD IDord-540855a0120c4351a54dd5ae22d9609f
Source noteuspto-grants-2015_07