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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792498Generated: November 4, 2026

HCID 22032377, compound → HCID 22031666, compound

https://huagongshe.com/reaction/1792498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22032377HCID 22032377—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
ProductHCID 22031666HCID 2203166681.3%

Reaction Steps

1.41 g of t-butyl 4-[hydroxy-(5-methylsulfanylthiophen-2-yl)-methyl]-piperidine-1-carboxylate (compound in Production Example 389) was dissolved in 40 mL acetone, and 14 g manganese dioxide was added thereto and stirred at room temperature for 24 hours. The reaction mixture was filtered through Celite, then the solvent was removed to give 1.14 g t-butyl 4-(5-methylsulfanylthiophen-2-carbonyl)piperidine-1-carboxylate, 5 mL of 4 N hydrogen chloride in ethyl acetate was added thereto, and the mixture was left for 1 hour. The solvent was removed, and the precipitated crystals were washed with ethyl acetate/ether, to give 0.75 g of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074801B1
Source datasetuspto-grants-2006_07
ORD IDord-d751c0626a6448e78cef8dabd2d464de
Source noteuspto-grants-2006_07