HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355342Generated: October 26, 2026
Sodium borohydride → 1-Nitro-2-phenylethane
https://huagongshe.com/reaction/355342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | beta-nitrostyrene, (E)- | HCID 5284459 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Nitro-2-phenylethane | HCID 80208 | 54.1% |
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 was 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05830870 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-28a296139c7544dcb942ea8c52facf62 |
|---|
| Source note | uspto-grants-1998_11 |
|---|