Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269690Generated: October 30, 2026

3-Nitrobenzaldehyde → HCID 15229832, compound

https://huagongshe.com/reaction/2269690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantTrimethyl orthoformateHCID 9005—
Reactant3-Amino-1-propanolHCID 9086—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 15229832HCID 15229832—

Reaction Steps

To a solution of m-nitrobenzaldehyde (94.23 mmol) and trimethylorthoformate (15.5 mL, 141 mmol) in MeOH (300 mL) is added dropwise 3-amino-1-propanol (7.21 mL, 94.23 mmol) at room temperature. The reaction is allowed to stir at room temperature for 5 hours followed by cooling to 0° C. in an ice bath. Sodium borohydride (3.56 g, 94.23 mmol) is added in two portions and when the bubbling stops the solvent is evaporated. The resulting residue is partitioned between ethyl acetate (75 mL) and water (75 mL). The aqueous layer is extracted twice with ethyl acetate (75 mL). The ethyl acetate extracts are collected and washed twice with Brine (50 mL), dried over MgSO4, filtered, and concentrated. Drying will give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329523B1
Source datasetuspto-grants-2001_12
ORD IDord-2472142dcec74e39854de1511547b75c
Source noteuspto-grants-2001_12