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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614893Generated: November 1, 2026

Toluene → HCID 43163816, compound

https://huagongshe.com/reaction/1614893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCyclopropylamineHCID 69828—
Reactant2-Bromo-5-methoxybenzaldehydeHCID 344480—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 43163816HCID 43163816—

Reaction Steps

In a flask fitted with a Dean-Stark trap was introduced 2-bromo-5-methoxybenzaldehyde (5.68 g, 26.41 mmol), cyclopropylamine (3.02 g, 52.83 mmol) and toluene (70 ml). The reaction mixture was stirred at room temperature for 1 hour and then at reflux for 4 hours. The solution was then concentrated to give a yellow oil to which was added methanol (30 ml). The reaction mixture was cooled on icebath followed by portionwise addition of sodium borohydride (2.00 g, 52.83 mmol). After complete addition, the reaction mixture was stirred 2 hours at room temperature, and then water (70 ml) was added. The crude product was isolated by extraction with dichloromethane and the combined organic phases were dried over sodium sulfate, filtered, and finally evaporated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765728B2
Source datasetuspto-grants-2014_07
ORD IDord-bea219235cc346bca6eb4e273a38fed3
Source noteuspto-grants-2014_07