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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927490Generated: October 30, 2026

Acetaldehyde → HCID 131728473, compound

https://huagongshe.com/reaction/1927490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 131728472HCID 131728472—
SolventMethanolHCID 887—
ProductHCID 131728473HCID 131728473—

Reaction Steps

Acetaldehyde (0.151 g, 3.4 mmol) was added to a solution of Example 92k (0.330 g, 0.68 mmol) in MeOH (10 mL) at 0° C. TFA (0.08 g, 0.68 mmol) was then added and stirring continued for 2 h. The reaction mixture was brought to room temperature, treated with sodium cyanoborohydride (0.108 g, 1.7 mmol) and allowed to stir for 4 h. It was concentrated, treated with aqueous sodium bicarbonate solution, water and extracted ethyl acetate. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography to obtain the title compound. Yield: 0.80 g, (51%); 1H NMR (CDCl3): δ 1.20 (t, 2H, CH2), 1.70 (t, 2H, CH2), 1.80 (t, 4H, 2CH2), 2.70 (s, 3H, CH3), 2.80 (s, 2H, CH2), 2.90 (m, 2H, CH2), 3.40 (q, 2H, CH2), 3.80 (t, 2H, CH2), 3.9 (s, 3H, OCH3), 4.8 (s, 2H, CH2), 6.8 (s, 2H, Ar), 8.10 (s, 1H, Ar), 8.4 (s, 1H, Ar); MS: m/e (ES−) 506 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183234B2
Source datasetuspto-grants-2012_05
ORD IDord-7041da9a900c4f4db743bbdc6966cb38
Source noteuspto-grants-2012_05