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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784832Generated: October 29, 2026

Sodium Thiosulfate → HCID 68842108, compound

https://huagongshe.com/reaction/1784832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68843555HCID 68843555—
SolventDichloromethaneHCID 6344—
ProductHCID 68842108HCID 68842108—

Reaction Steps

To [3-bromo-5-(4-methoxy-benzyloxy)-phenyl]-(6-methoxy-pyridin-3-yl)-methanol in methylene chloride (5 mL) at room temperature was added Dess-Martin reagent. The resulting reaction mixture was stirred at room temperature for 1 h. Sat. NaHCO3 and Na2S2O3 were then added and the stirring was continued until both phases become clear. The organic phase was separated, dried and concentrated to provide [3-bromo-5-(4-methoxy-benzyloxy)-phenyl]-(6-methoxy-pyridin-3-yl)-methanone which was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504401B2
Source datasetuspto-grants-2009_03
ORD IDord-2b65fbb62b1847dba2e7c16757c6dac1
Source noteuspto-grants-2009_03