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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860496Generated: November 1, 2026

Sodium hydride → HCID 57444583, compound

https://huagongshe.com/reaction/860496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantO-(Diphenylphosphinyl)hydroxylamineHCID 10955453—
ReactantHCID 57444580HCID 57444580—
SolventDimethylformamideHCID 6228—
ProductHCID 57444583HCID 5744458389.9%

Reaction Steps

To a solution of methyl 2-bromo-4-[(5-ethyl-1H-pyrrol-2-yl)carbonyl]benzoate (330 mg) in N,N-dimethylformamide (5 mL) was added 60% sodium hydride in oil (58.4 mg) in an ice-bath over 5 miutes. After stirring for 1 hour, (aminooxy)(diphenyl)phosphine oxide (340 mg) was added portionwise over 40 minutes. The resulting mixture was stirred for 1 hour in the bath. The reaction was quenched by adding water (10 mL). The mixture was partitioned between ethyl acetate and water. The organic layer was washed with water (two times) and brine, dried over magnesium sulfate, and evaporated. The residue was dissolved in ethyl acetatec-hexane (1-5), and to the solution was added silicagel. The mixture was filtered, and the filtrate was evaporated to give methyl 4-[(1-amino-5-ethyl-1H-pyrrol-2-yl)carbonyl]-2-bromobenzoate as an orange solid (310 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-07b8067708e14551b146c3a1e1d5bd67
Source noteuspto-grants-2006_12