Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628569Generated: October 30, 2026

Acetic Acid → HCID 68772648, compound

https://huagongshe.com/reaction/1628569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehydeHCID 177—
ReactantSodiumacetoxyborohydrideHCID 23670382—
ReactantHCID 68773584HCID 68773584—
SolventMethanolHCID 887—
ProductHCID 68772648HCID 68772648—

Reaction Steps

To a suspension of methyl 3-{7-amino-2-[(2,4-dichlorophenyl) (hydroxy)methyl]-1H-benzimidazol-1-yl}propanoate (6.00 g, 14.7 mmol) and acetic acid (7.4 mL) in methanol (147 mL) was added acetaldehyde (4.95 mL, 88.2 mmol) at 0° C. After 30 min, sodium acetoxyborohydride. (18.7 g, 88.2 mmol) was added. After 2 h, the reaction mixture was quenched with water, concentrated in vacuo, diluted with ethyl acetate, washed with aqueous sodium hydroxide (1 M) and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a 10-30% ethyl acetate/n-hexane gradient mixture to give the title compound as a colorless amorphous (6.30 g, 13.6 mmol, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-37f3ccf433bd407c882f67eb960a469b
Source noteuspto-grants-2014_07