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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628401Generated: November 1, 2026

Acetaldehyde → HCID 68761561, compound

https://huagongshe.com/reaction/1628401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodiumacetoxyborohydrideHCID 23670382—
ReactantHCID 68763200HCID 68763200—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductHCID 68761561HCID 68761561104.2%

Reaction Steps

To a solution of ethyl 3-{7-amino-2-[(2,4-dichlorophenyl)amino]-1H-benzimidazol-1-yl}propanoate (Reference Example 27; 214 mg, 0.544 mmol) in methanol (5.5 mL) and acetic acid (0.110 mL) was added acetaldehyde (0.204 mL, 3.27 mmol) at 0° C. The resultant mixture was stirred at 0° C. for 30 min. To the reaction mixture was added sodium acetoxyborohydride (692 mg, 3.27 mmol) at 0° C. After the resultant mixture was stirred at room temperature for 12 hr, the mixture was diluted with aqueous saturated sodium hydrogen carbonate and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on NH-silica gel eluting with ethyl acetate to give the title compound as a solid (255 mg, 0.567 mmol, quant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-bf4a5e9f2b4c44728f65700bf8e10de9
Source noteuspto-grants-2014_07