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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603433Generated: October 31, 2026

Sodium borohydride → 1-Nitro-2-phenylethane

https://huagongshe.com/reaction/1603433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantbeta-nitrostyrene, (E)-HCID 5284459—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
Product1-Nitro-2-phenylethaneHCID 8020854.1%

Reaction Steps

To a stirring mixture of trans-β-nitrostyrene (5.25 g, 0.035 mol) and silica gel (10 g, 230-400 mesh) in chloroform (400 mL) and isopropanol (75 mL) at room temperature, was slowly added sodium borohydride (5.50 g, 0.145 mol) over a period of 45 min. The reaction mixture was stirred for an additional 15 min and then carefully quenched with 10% hydrochloric acid (20 mL). Separated solid wins filtered and washed with chloroform (50 mL). Combined filtrate and washing was washed with water (1×20 mL), brine (1×20 mL) and dried over anhydrous sodium sulfate. Solvent evaporation at reduced pressure gave a crude material which was purified by flash chromatography (silica gel, 8% ethyl acetate-hexane) to give 2.86 g of 1-nitro-2-phenylethane as a colorless oil (spicy odor); Rf (10% ethyl acetate in hexane): 0.40; 1H-NMR (300 MHz, CDCl3) 7.40-7.20 (m, 5H), 4.60 (t, 2H), 3.30 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990083
Source datasetuspto-grants-1999_11
ORD IDord-f91355ffcfa645e7aef12dca33e245e2
Source noteuspto-grants-1999_11