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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628480Generated: November 1, 2026

Acetaldehyde → HCID 68773304, compound

https://huagongshe.com/reaction/1628480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodiumacetoxyborohydrideHCID 23670382—
ReactantHCID 68766832HCID 68766832—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductHCID 68773304HCID 6877330490%

Reaction Steps

To a solution of methyl 5-{7-amino-2-[(2,4-dichlorophenyl)amino]-1H-benzimidazol-1-yl}pentan-1-ol (Reference Example 112; 308 mg, 1.85 mmol) in methanol (8 mL) and acetic acid (0.160 mL) was added acetaldehyde (0.304 mL, 4.88 mmol) at 0° C. The resultant mixture was stirred at 0° C. for 30 min. To the reaction mixture was added sodium acetoxyborohydride (1.03 g, 4.86 mmol) at 0° C. After the resultant mixture was stirred at room temperature for 14 hr, the mixture was diluted with aqueous 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 silica gel eluting with ethyl acetate to give the title compound as a solid (317 mg, 0.729 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-b5e925c76052402a85de3e90d9e4df64
Source noteuspto-grants-2014_07