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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107369Generated: October 25, 2026

Benzaldehyde → 2-Nitro-1-phenylbutan-1-ol

https://huagongshe.com/reaction/2107369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1-NitropropaneHCID 7903—
ReactantTriethylamineHCID 8471—
ReactantEthyl aluminium dichlorideHCID 16686341—
SolventDichloromethaneHCID 6344—
Product2-Nitro-1-phenylbutan-1-olHCID 22612329%

Reaction Steps

To a solution of nitropropane (0.45 g, 0.005 moles) in dichloromethane (25 mL) at 0° C. was added triethylamine (0.67 mL, 0.005 moles) followed by ethyl aluminum dichloride (1.0 M in hexane, 5 mL, 0.005 moles). After 15 minutes benzaldehyde (0.5 mL 0.005 moles) was added and the solution allowed to warm to room temperature. After a further 3 hours the reaction was cooled in ice to a temperature of 5° C. and quenched with pH 7.0 phosphate buffer. The organic layer was separated, dried and evaporated in vacuo. Flash column chromatography [SiO2, 6:1 hexane, Et2O] gave 1-phenyl-2-nitro-1-butanol (0.28 g, 29%) Erythro:threo ratio 1:1.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933505
Source datasetuspto-grants-1990_06
ORD IDord-d8a18e7ed19a42ab9a50f5bb802ded73
Source noteuspto-grants-1990_06