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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264544Generated: October 31, 2026

Acetic Acid → HCID 16737504, compound

https://huagongshe.com/reaction/2264544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-azetidinecarboxylic AcidHCID 93192—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 59595889HCID 59595889—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 16737504HCID 1673750465%

Reaction Steps

A mixture of 4-(5-isobutylbenzofuran-2-yl)benzaldehyde (30 mg, 0.11 mmol), acetic acid (10 μL, 0.15 mmol) and azetidine-3-carboxylic acid (16 mg, 0.16 mmol) in DCM/MeOH (1:1, 2 mL) was stirred at room temperature for 1 h. Sodium cyanoborohydride (3.4 mg, 0.054 mmol) was added and the reaction mixture was stirred for 3 h at room temperature. After concentration of solvent under reduced pressure, the resulting residue was dissolved in an aliquot of DMSO and purified by reverse phase preparative HPLC (Phenomenex reverse phase Luna 5μ C18(2) column, 60×21.2 mm ID) to yield the desired final product (25.6 mg, 65% yield) as a colorless film: >95% purity by LCMS, ESI-MS: 364.0 (M+H)+, 1H NMR (400 MHz, CD3OD) δ 7.99 (d, 2H), 7.55 (d, 2H), 7.42 (d, 1H), 7.39 (s, 1H), 7.24 (s, 1H), 7.12 (dd, 1H), 4.44 (s, 2H), 4.33(d, 4H), 3.68 (m, 1H), 2.57 (d, 2H), 1.90 (m, 1H), 0.92 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855193B2
Source datasetuspto-grants-2010_12
ORD IDord-da41a2c1a49f4ab0bd87cf142626ebdc
Source noteuspto-grants-2010_12