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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172496Generated: November 2, 2026

Acetaldehyde → HCID 131728467, compound

https://huagongshe.com/reaction/1172496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 131728466HCID 131728466—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 131728467HCID 131728467—

Reaction Steps

Trifluoroacetic acid (0.03 mL, 0.4 mmol) was added to mixture of Example 84k (0.2 g, 0.40 mmol) and acetaldehyde (0.115 mL, 2 mmol) in dry methanol (10 mL) at 0° C. The reaction mixture was stirred at room temperature in an atmosphere of nitrogen for 1.5 h. It was treated with sodium cyanoborohydride (0.064 g, 1 mmol), stirred for 1.5 h, treated with cold water and extracted with ethyl acetate. The organic layer was washed with water, brine, dried and purified using flash chromatography (silica gel, ethyl acetate/pet ether) to obtain the title compound as a white solid. Yield: 0.285 g, (68.69%); 1H NMR (DMSO-d6): δ 1.1 (t, 6H, 2CH3), 2.60-2.69 (m, 4H, 2CH2), 2.70 (s, 3H, CH3), 3.30-3.40 (m, 4H, 2CH2), 3.70 (s, 2H, CH2), 3.95 (s, 3H, OCH3), 4.65 (s, 2H, CH2), 6.25-6.85 (m, 3H, Ar), 6.65 (s, 1H, Ar), 7.45 (s, 1H, Ar), 8.10 (s, 1H, Ar), 8.50 (s, 1H, Ar); MS: m/e (CI+) 547 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834001B2
Source datasetuspto-grants-2010_11
ORD IDord-810e2702c81d4ba3b1cb84d7a08fbf79
Source noteuspto-grants-2010_11