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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691540Generated: November 1, 2026

Acetic Acid → HCID 66908116, compound

https://huagongshe.com/reaction/1691540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4'-(2-Ethoxyethoxy)-2',6'-dimethylbiphenyl-3-carbaldehydeHCID 23111722—
ReactantEthyl 2-(4-amino-2-fluorophenyl)cyclopropane-1-carboxylateHCID 59364058—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 66908116HCID 6690811686%

Reaction Steps

A mixture of 4′-(2-ethoxyethoxy)-2′,6′-dimethyl-3-biphenylcarbaldehyde (0.313 g, 1.05 mmol), ethyl 2-(4-amino-2-fluorophenyl)cyclopropanecarboxylate (0.234 g, 1.05 mmol), acetic acid (0.126 g, 2.10 mmol) and 1,2-dichloroethane (5 mL) was stirred under a nitrogen atmosphere at room temperature for 3 hr. Sodium triacetoxyborohydride (0.445 g, 2.10 mmol) was added to the reaction mixture by small portions, and the mixture was stirred for 3.5 hr. The reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-30:70) to give the title compound (0.456 g, yield 86%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153694B2
Source datasetuspto-grants-2012_04
ORD IDord-b5ddb9abaaeb432b9bf4fab26363443d
Source noteuspto-grants-2012_04