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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196248Generated: October 25, 2026

tert-Butyl hydroperoxide → HCID 67609461, compound

https://huagongshe.com/reaction/2196248

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantSodium ThiosulfateHCID 24477—
ReactantAmmonia hydroxideHCID 21862953—
Reactant(R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thioneHCID 86667520—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
ProductHCID 67609461HCID 67609461—

Reaction Steps

(R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thione (2.86 g, 7.77 mmol) was dissolved in 7M NH3 in methanol (50 ml). Tert-Butylhydroperoxide (9.41 ml, 78 mmol) and ammonia hydroxide (25% sol., 21.2 ml, 136 mmol) were added and the reaction was stirred at r.t. for 2 hrs. Upon completion, 50 ml half-saturated Na2S2O3 solution was added to the reaction and the product was extracted with ethyl acetate. The organic phases were washed with water and brine, combined and dried over Na2SO4. Volatiles were removed under reduced pressure, yielding the title compound as yellowish solid. 1H-NMR (360 MHz, DMSO-d6): 8.34 (s, 1H), 8.25 (s, 1H), 8.12 (s, 1H), 5.85 (br, 2H), 4.01 (m, 1H), 3.80 (m, 1H), 3.55 (m, 1H), 1.38 (s, 3H); MS: 314 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338413B1
Source datasetuspto-grants-2012_12
ORD IDord-f5c107543764477998a5419dcec61983
Source noteuspto-grants-2012_12