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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487278Generated: November 2, 2026

Acetone → HCID 103750657, compound

https://huagongshe.com/reaction/1487278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
Reactant2-Bromo-5-fluoroanilineHCID 2773317—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductHCID 103750657HCID 103750657—

Reaction Conditions

Temperature20 °C

Reaction Steps

2-bromo-5-fluoroaniline E-1.7″″″ (2.00 g; 10.53 mmol) is suspended in 20 ml DCM and propan-2-one (1.55 ml; 21.05) is added and the reaction mixture is stirred for 16 at 20° C. Afterwards sodium triacetoxyborohydride (4.69 g; 21.05 mmol) is added and the reaction mixture is stirred for 48 h at 20° C. The reaction mixture is poured into water and extracted with DCM. The combined organic layer is dried over MgSO4 the solid materials are filtered off and HCl in dioxane is added until the pH value is below 2. The solvents are concentrated under reduced pressure. The crude product is purified using reversed phase chromatography (Method: prep. HPLC1). Product containing fractions are combined and extracted with DCM. To the organic layer HCl in dioxane is added until the pH value is below 2. The solvents are concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428515B2
Source datasetuspto-grants-2016_08
ORD IDord-f4c62be1dc4a4d1c97f0bfb47a5acd5d
Source noteuspto-grants-2016_08