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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452628Generated: October 31, 2026

Hydrogen Peroxide → HCID 57526810, compound

https://huagongshe.com/reaction/1452628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
ReactantHCID 57526828HCID 57526828—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57526810HCID 5752681065%

Reaction Steps

To a tetrahydrofuran (23 mL) solution containing tert-butyl (6-allyl-5-chloropyrazolo[1,5-a]pyrimidin-7-yl)(4-ethoxyphenyl)carbamate (3.0 g, 7.0 mmol), borane-dimethyl sulfide complex (2 mol/L tetrahydrofuran solution, 5.6 mL, 23 mmol) was added over 30 min with ice-cooling. This mixture was stirred at room temperature for 2 hr and then again cooled on ice. Here, 1 mol/L aqueous sodium hydroxide (11.2 mL, 11.2 mmol) was added over 20 min, and hydrogen peroxide (30% aqueous solution, 0.81 mL, 8.4 mmol) was added. The resultant mixture was stirred for 1 hr. After the reaction, the reaction mixture was extracted with ethyl acetate. The combined ethyl acetate layer was washed with brine and dried over sodium sulfate. After the sodium sulfate was filtered off, the solvent was distilled off and the residue was purified with column chromatography (20% ethyl acetate-hexane) to obtain the title compound (2.02 g, yield 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473694B2
Source datasetuspto-grants-2009_01
ORD IDord-0f0cc1a3bfc1400caa12018e093465b0
Source noteuspto-grants-2009_01