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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128575Generated: November 1, 2026

Sulfur Dioxide → HCID 19374696, compound

https://huagongshe.com/reaction/128575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantHCID 19374699HCID 19374699—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19374696HCID 19374696—

Reaction Conditions

Temperature-78 °C

Reaction Steps

The product from step A (1.5 g, 6.30 mmol) was dissolved in dry THF (60 mL) and cooled to -78° C. under nitrogen. n-Butyllithium (5.33 mL of a 2.5 M solution in hexanes, 13.3 mmol) was added dropwise and the mixture was stirred for 1h at -78° C. A stream of sulfur dioxide gas was passed through the surface of the mixture for 15 min and then the mixture was allowed to warm to room temperature. Evaporation of the volatiles provided a residue which was dissolved in water (60 mL) to which was added sodium acetate trihydrate (2.59 g, 19.06 mmol). This solution was cooled to 0° C. and hydroxylamine-O-sulfonic acid (2.15 g, 19.06 mmol) was added followed by stirring for 18h. The reaction mixture was extracted with ethyl acetate (2×50 mL). The combined extracts were dried over MgSO4 and concentrated to a crude oil which was purified by flash column chromatography (silica, hexane-ethyl acetate gradient) to lead to a white solid (1 g, 50%). decomposition: >163° C. 1H NMR (DMSO-d6): δ:2.48 (3H, 1s, CH3); 8.17 (2H, s, NH2 exchangeable).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464831
Source datasetuspto-grants-1995_11
ORD IDord-949a810f67bf4f63bde4ce0391c6ee6d
Source noteuspto-grants-1995_11