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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400560Generated: October 30, 2026

Triethylamine → HCID 61286981, compound

https://huagongshe.com/reaction/2400560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 55139138HCID 55139138—
SolventEthanolHCID 702—
ProductHCID 61286981HCID 61286981—

Reaction Steps

A solution of 4-[(tetrahydro-2H-pyran-4-yloxy)methyl]benzonitrile (Step 1, 780 mg, 3.59 mmol), hydroxylamine hydrochloride (549 mg, 7.90 mmol) and triethylamine (1.10 mL, 7.90 mmol) in ethanol (20 mL) was stirred and heated at reflux for 1 h. After being cooled to rt, the reaction mixture was evaporated to dryness. The resulting material was treated with ethyl acetate, and the solid was filtered off. The ethyl acetate solution was washed with water and saturated sodium chloride solution, dried with anhydrous magnesium sulfate and filtered. After evaporation of the solvent, the crude product was stirred in hexane and filtered. After evaporation of the solvent, the title compound was obtained (857 mg, 95%): 1H NMR (400 MHz, CDCl3) δ 7.55 (d, 2H), 7.40 (d, 2H), 4.81 (s, 2H), 4.06-3.99 (dd, 2H), 3.81 (d, 2H), 3.48-3.40 (m, 2H), 2.15-2.02 (m, 1H), 1.78-1.72 (dd, 2H), 1.52-1.40 (m, 2H); ES-MS m/z 251, HPLC RT (Method E) 0.56 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796253B2
Source datasetuspto-grants-2014_08
ORD IDord-fff92d16b396442e98a2a403fbcc33bb
Source noteuspto-grants-2014_08