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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397105Generated: October 25, 2026

Sodium Thiosulfate → 1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/397105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTempolHCID 137994—
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1,4-Dihydroxy-2,2,6,6-tetramethylpiperidineHCID 5395—

Reaction Steps

A mixture of bisnoralcohol (I, 4 g), 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (4-hydroxy-TEMPO, 10 mg), potassium bromide (133 mg), sodium bicarbonate (133 mg), dichloromethane (14 ml) and water (2.2 ml) are cooled to 1°. While maintaining this temperature, aqueous sodium hypochlorite (14%, 6.3 ml) is added over a five hr period. The reaction is complete and aqueous sodium thiosulfate is added, the two phases were separated, and the bisnoraldehyde product is crystallized by replacing the dichloromethane with heptane to give the title compound, mp=153-154°; NMR (CDCl3) 9.56, 5.73, 2.2-2.5, 1.2-2.1, 1.20, 1.10, 0.79 δ; [α]D22=+83.4° (methylene chloride, c=1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608220B1
Source datasetuspto-grants-2003_08
ORD IDord-619431b9741c4897aae74f258ed06159
Source noteuspto-grants-2003_08