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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913553Generated: November 3, 2026

Acetone → HCID 178457142, compound

https://huagongshe.com/reaction/1913553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178463402HCID 178463402—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178457142HCID 178457142100%

Reaction Steps

1-(4-Phenyl-1H-imidazol-2-yl)-ethylamine (0.20 g, 1.07 mmol) and acetone (0.062 g, 1.07 mmol) were mixed in 1,2-dichloroethane (4 mL), followed by the addition of NaBH(OAc)3 (0.34 g, 1.61 mmol). The resulting mixture was stirred at rt for 3 h. The reaction was quenched with saturated NaHCO3 solution. The mixture was extracted with EtOAc and the combined extracts were dried over Na2SO4. Filtration followed by evaporation to dryness under reduced pressure gave the crude isopropyl-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amine (0.23 g, 100%) which was used for the next reaction without further purification. 1H NMR (300 MHz, CDCl3): δ 1.10 (3H, d), 1.18 (3H, d), 1.57 (3H, d), 2.86 (1H, m), 4.32 (1H, m), 7.24 (2H, m), 7.36 (2H, m), 7.69 (2H, m). MS (ES+): 230.2 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609709B2
Source datasetuspto-grants-2013_12
ORD IDord-dad6aad7bdba420bbe184f738127c18e
Source noteuspto-grants-2013_12