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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 424288Erstellt: 23. Oktober 2026

Acetic Acid → 1-Nitro-2-phenylethane

https://huagongshe.com/de/reaction/424288

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBeta-NitrostyreneHCID 7626—
EduktSodium borohydrideHCID 4311764—
Lösungsmittel1,4-DioxaneHCID 31275—
LösungsmittelDioxan ethanolHCID 22560076—
Produkt1-Nitro-2-phenylethaneHCID 8020883%

Reaktionsschritte

In a 500 mL two-necked flask equipped with a thermometer and a pressure-equalizing dropping funnel, NaBH4 (5.33 g, 0.140 mol) was suspended in 1,4-dioxane/ethanol (100 mL/30 ml). ≈-Nitrostyrene (3, 10.0 g, 67.0 mmol) in 1,4-dioxane (100 mL) was added dropwise to the solution over 45 minutes, keeping the temperature below 30° C. A fine slurry formed during the addition. After the addition the reaction mixture was stirred overnight, then ice/water (125 mL) was added, and a 50% solution of acetic acid was added to neutralize excess NaBH4; the clear solution was then concentrated in vacuo and the residue was dissolved in water and extracted twice with CH2Cl2. The organic phase was washed with water (2×30 mL) and brine (1×30 mL), dried (Na2SO4), filtered and evaporated in vacuo obtaining 4 (8.40 g, 83%) as yellow oil. ESI-MS: 152 (MH+) (Calc. for C8H9NO2: 151).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08105567B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-360d644d2bd343edab5d583f6ce741f3
Quellennotizuspto-grants-2012_01