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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191636Generated: November 1, 2026

Sodium hydride → HCID 69640386, compound

https://huagongshe.com/reaction/1191636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-Boc-3-(4-cyanophenyl)oxaziridineHCID 2725038—
ReactantHCID 178418934HCID 178418934—
SolventDimethylformamideHCID 6228—
ProductHCID 69640386HCID 6964038657%

Reaction Steps

4-Bromo-1H-imidazole (3.2 g, 21.8 mmol) was weighed into a 500 mL round bottomed flask equipped with a magnetic stir bar under a nitrogen atmosphere. Anhydrous N,N-dimethylformamide (DMF, 12 mL) was added and the mixture was placed on ice. After 10 minutes the mixture was treated with sodium hydride (0.840 g, 21.0 mmol 60% dispersion in oil). After 5 minutes, the ice bath was removed and the reaction warmed to room temperature. After 15 minutes of vigorous stirring the ice bath was re-inserted and 3-(4-cyano-phenyl)-oxaziridine-2-carboxylic acid tert-butyl ester (1.92 g, 7.80 mmol) was added. The reaction was vigorously stirred for 5 minutes and the ice bath was removed. After 5 minutes the mixture was diluted with saturated sodium bicarbonate and extracted with ethyl acetate. The organics were washed with dilute sodium carbonate, dried over sodium sulfate, and concentrated. The residue was purified using silica gel chromatography (0-5% methanol/dichloromethane) to afford the title compound (1.16 g, 4.43 mmol, 57%) as a yellow oil: 1H NMR (400 MHz, CDCl3) δ 9.22 (s, 1H), 7.36 (d, J=1.5 Hz, 1H), 6.97 (d, J=1.5 Hz, 1H), 1.48 (s, 9H); ESIMS m/z 262 ([M]+), 260 ([M−2]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680121B2
Source datasetuspto-grants-2014_03
ORD IDord-6bcb903c900b41b3becd72a94757d053
Source noteuspto-grants-2014_03