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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516654Generated: October 30, 2026

P-Toluenesulfonylhydrazide → HCID 117833149, compound

https://huagongshe.com/reaction/516654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonylhydrazideHCID 15303—
ReactantSodium bicarbonate waterHCID 86585896—
ReactantHCID 117833033HCID 117833033—
SolventBenzeneHCID 241—
ProductHCID 117833149HCID 11783314962%

Reaction Steps

p-Toluenesulfonyl hydrazine (6.37 g, 34.2 mmol) was added to a benzene solution (115 ml) of N-tert-butoxycarbonyl-1,5-dimethyl-9-azabicyclo[3.3.1]nonan-3-one (3.04 g, 11.4 mmol), and the mixture was heated under reflux for 6 h with a Dean-Stark device. After adding saturated sodium bicarbonate water under ice-cooled condition, the ice-cooled reaction liquid was extracted with ethyl acetate, washed with saturated brine, and dried over magnesium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography to give N-tert-butoxycarbonyl-1,5-dimethyl-3-(tosylhydrazono)-9-azabicyclo[3.3.1]nonane (3.07 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09114390B2
Source datasetuspto-grants-2015_08
ORD IDord-06f65933c760490ba121feca809619fb
Source noteuspto-grants-2015_08