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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628582Generated: November 3, 2026

Acetaldehyde → HCID 86632922, compound

https://huagongshe.com/reaction/1628582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86632921HCID 86632921—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86632922HCID 8663292274%

Reaction Steps

To a solution of tert-butyl (2-{7-amino-2-[(2,4-dichlorophenyl) (hydroxy)methyl]-1H-benzimidazol-1-yl}ethyl)carbamate (5.00 g, 11.1 mmol) in methanol (110 mL) and acetic acid (5.5 mL) was added acetoaldehyde (4.15 mL, 66.6 mmol) at 0° C. The resultant mixture was stirred at 0° C. for 30 min. To the reaction mixture was added sodium triacetoxyborohydride (14.1 g, 66.5 mmol) at 0° C. After the resultant mixture was stirred at room temperature for 3 h, the mixture was diluted with aqueous sodium hydrogen carbonate and 8N aqueous sodium hydroxide, and extracted with ethyl acetate. The combined organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a 20-50% ethyl acetate/n-hexane gradient mixture to give a colorless solid (4.15 mg, 8.18 mmol, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-31765e9c856a41ef94bf87c767e135bb
Source noteuspto-grants-2014_07