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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403283Generated: October 31, 2026

Sodium borohydride → HCID 86671392, compound

https://huagongshe.com/reaction/2403283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58370509HCID 58370509—
ReactantHCID 80146944HCID 80146944—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86671392HCID 8667139294%

Reaction Steps

To a stirred suspension of the mixture of 2-bromo-1-(3-methyl-4-nitrophenyl)ethanone and 2-chloro-1-(3-methyl-4-nitrophenyl)ethanone (6.23 g) in ethanol (100 ml) at 5° C. was added portionwise over 5 min NaBH4 (913 mg). The reaction mixture was then stirred at room temperature for 1 hour to afford a dark yellow solution. TLC analysis showed the reaction was complete. Sodium methoxide (652 mg) was then added and the reaction mixture was stirred at room temperature overnight. TLC analysis showed a small amount of starting material remaining and so the reaction mixture was stirred at 40° C. for 1 h. The reaction mixture was then poured into EtOAc and extracted with saturated brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to afford (RS)-2-(3-methyl-4-nitrophenyl)oxirane (4.63 g, 94% over 2 steps) as a yellow oil. MS (EI): 179 (M+), 164 ([M-CH3]+), 162 [M-OH]+), 132 [M-OH—NO]+), 103, 77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-7ec11e01cab84786a9d7129f263441bc
Source noteuspto-grants-2014_08