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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443626Generated: November 1, 2026

Acetic Acid → HCID 68564972, compound

https://huagongshe.com/reaction/1443626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPhthalimide, N-(2-formylethyl)-HCID 75525—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 45588680HCID 45588680—
SolventDichloromethaneHCID 6344—
ProductHCID 68564972HCID 68564972—

Reaction Steps

To a solution of 1-(1-benzyl-1H-benzimidazol-2-yl)-2-methyl-propylamine (160 mg, 0.56 mmol) and 3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionaldehyde (114 mg, 0.56 mmol) in dry DCM (3 ml) at room temperature, was added sodium triacetoxyborohydride (119 mg, 0.56 mmol). After 10 minutes, acetic acid (34 μl, 0.56 mmol) was added to the reaction mixture. The mixture was stirred at room temperature for 1 hour. The solvent was removed in vacuo and the solid was dissolved in ethyl acetate. The organic layer was washed with saturated NaHCO3, dried over MgSO4, filtered and the filtrate was concentrated in vacuo. The crude product was purified by flash chromatography to give material that was used in Example 5g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662581B1
Source datasetuspto-grants-2010_02
ORD IDord-1e1e979e48404e939c081ca120585047
Source noteuspto-grants-2010_02