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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931129Generated: October 31, 2026

Sodium hydride → HCID 178449911, compound

https://huagongshe.com/reaction/1931129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-tert-butylhydroxylamineHCID 98586—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butylhydroxylamine acetateHCID 9877417—
ReactantHCID 178441918HCID 178441918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178449911HCID 178449911—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-tert-butylhydroxylamine (133 mg, 1.50 mmol) (prepared from commercially available N-tert-butylhydroxylamine acetate (Aldrich) by adding saturated sodium bicarbonate solution and extracting the free base with ethyl ether) in anhydrous THF (10 mL) was added sodium hydride (53.9 mg, 1.35 mmol). The mixture was stirred at 0° C. for 20 min. A solution of Example 151A (310 mg, 0.75 mmol) in THF (4 mL) was added and the mixture was stirred at 22° C. for 5 hours. The solvent was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried with MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 using an Analogix® Intelliflash280™ (Hexanes-EtOAc: 0-50% gradient) to give the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.22 (s, 9H), 1.42 (s, 9H), 2.23-2.37 (m, 2H), 2.48 (t, J=7.1 Hz, 2H), 4.54 (t, J=6.5 Hz, 2H), 5.75 (s, 1H), 7.61 (dd, J=8.7, 2.4 Hz, 1H), 7.83 (d, J=8.7 Hz, 1H), 8.28 (d, J=2.4 Hz, 1H); MS (ESI) m/z 484 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188135B2
Source datasetuspto-grants-2012_05
ORD IDord-c3dbfd8a917a49fd9f2475c0d8e3fe3b
Source noteuspto-grants-2012_05