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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628587Generated: October 31, 2026

Acetaldehyde → HCID 86632927, compound

https://huagongshe.com/reaction/1628587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86632926HCID 86632926—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86632927HCID 8663292790.4%

Reaction Steps

To a solution of tert-butyl (3-{7-amino-2-[(2,4-dichlorophenyl) (hydroxy)methyl]-1H-benzimidazol-1-yl}propyl)carbamate (3.00 g, 6.45 mmol) in methanol (65 mL) and acetic acid (3.3 mL) was added acetoaldehyde (2.41 mL, 38.7 mmol) at 0° C. The resultant mixture was stirred at 0° C. for 30 min. To the reaction mixture was added sodium triacetoxyborohydride (8.20 g, 38.7 mmol) at 0° C. After the resultant mixture was stirred at 0° C. for 3 h, the mixture was diluted with aqueous sodium hydrogen carbonate and 1N aqueous sodium hydroxide, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a ethyl acetate to give a crude solid, which was washed with diisopropyl ether to give the title compound as a colorless solid (3.04 g, 5.83 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-abb17194bdde4b029c09937e942d7593
Source noteuspto-grants-2014_07