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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850313Generated: October 25, 2026

P-Toluenesulfonamide → 6-Tosyl-2-oxa-6-azaspiro[3.3]heptane

https://huagongshe.com/reaction/1850313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonamideHCID 6269—
ReactantPotassium HydroxideHCID 14797—
ReactantPentaerythritol tribromideHCID 15206—
SolventEthanolHCID 702—
Product6-Tosyl-2-oxa-6-azaspiro[3.3]heptaneHCID 2331989163%

Reaction Steps

To a solution of 3-bromo-2,2-bis(bromomethyl)propanol (127) (3.25 g, 10 mmol) and potassium hydroxide (1.12 g, 20 mmol, in 10 mL water) in EtOH (20 mL) were added toluene-4-sulfonamide (3.76 g, 22 mmol). The reaction mixture was refluxed for 2 h, evaporated to remove EtOH then diluted with EAOAc (20 mL), washed with H2O (20 mL). The organic layer was washed with brine (20 mL), dried over Na2SO4, and filtered, evaporated to give the product to give 6-(toluene-4-sulfonyl)-2-oxa-6-aza-spiro[3.3]heptane (128) (1.6 g, 6.3 mmol, yield: 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-9a27ba83252e4f7291dd076301e982ea
Source noteuspto-grants-2015_02