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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435059Generated: November 4, 2026

Isoamylamine → HCID 57937835, compound

https://huagongshe.com/reaction/1435059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Bromo-2,6-difluorobenzaldehydeHCID 2773290—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 57937835HCID 57937835—

Reaction Steps

4-Bromo-2,6-difluoro-benzaldehyde (I-1a: 30 g) and isoamyl amine (13 g) were combined in dichloroethane (1 L) at ambient temperature. After stirring for 2 hours, sodium triacetoxyborohydride (144 g) was added to the reaction mixture. After stirring overnight, the reaction mixture was treated with a 2 M aqueous potassium hydroxide solution. The layers were separated and the organic phase dried over magnesium sulfate before being filtered and concentrated with a rotary evaporator to provide the title compound (I-1b) as an oil, which was used in the subsequent transformation without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615651B2
Source datasetuspto-grants-2009_11
ORD IDord-9a8360b127c244119525959f273ff1a5
Source noteuspto-grants-2009_11