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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859846Generated: October 25, 2026

Hydrogen Peroxide → 1H-Isophosphindole, 2-(1,1-dimethylethyl)-2,3-dihydro-, 2-oxide

https://huagongshe.com/reaction/859846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactanttert-ButylphosphineHCID 123165—
Reactant1,5-Dihydro-benzo[e][1,3,2]dioxathiepine 3,3-dioxideHCID 11117056—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1H-Isophosphindole, 2-(1,1-dimethylethyl)-2,3-dihydro-, 2-oxideHCID 1143571694%

Reaction Steps

To a solution of tert-butyl phosphine (1.40 mL, 11.5 mmol) in THF (40 mL) was added dropwise n-BuLi (11.5 mmol) at −78° C. The resulting yellow solution was allowed to warm to rt and stirred at rt for 1 h. A solution of 40 (2.29 g, 11.5 mmol) in THF (20 mL) was added at −78° C. via cannula. The resulting solution was allowed to warm to rt and stirred at rt for 5 h. After being cooled to −78° C. again, n-BuLi (11.5 mmol) was added dropwise. The reaction mixture was warmed to rt and stirred overnight. 2.5 mL H2O2 (30% aq.) was added at 0° C. After being stirred at 0° C. for 1 h, the reaction was quenched with saturated Na2SO3 solution (10 mL) at 0° C. for 1 h. After usual workup, the crude product was purified by recrystallization (CH2Cl2 and hexane) to give 50 as white crystals (2.26 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153809B2
Source datasetuspto-grants-2006_12
ORD IDord-008eec4e04014a55980bf6a7c5569126
Source noteuspto-grants-2006_12