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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781166Generated: October 31, 2026

3-Methoxyphenethylamine → HCID 19069351, compound

https://huagongshe.com/reaction/1781166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyphenethylamineHCID 74866—
ReactantBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 19069351HCID 1906935176.2%

Reaction Steps

A solution of 4-benzoxybenzaldehyde (2.5 g, 12.6 mmol), 3-methoxyphenethylamine (1.9 g, 12.6 mmol), a catalytic amount of p-toluenesulfonic acid monohydrate in absolute ethanol (12 mL) was stirred at 80° C. for 1.5 hours. After cooling to room temperature, NaBH4 (0.49 g, 13.0 mmol) was added in portions. The reaction mixture was stirred at 80° C. for 1 hour, then cooled to room temperature, and the ethanol was removed in vacuo. Water was added to the residue and the mixture was extracted with ethyl acetate. The combined extracts were washed with saturated NaCl, dried over MgSO4, filtered, and the solvent removed in vacuo to afford a colorless oil which was purified by silica gel chromatography eluting with 20% ethyl acetate in hexane saturated with NH3 to afford the title compound (3.2 g, 76%) as a colorless oil. MS (DCl/NH3) m/e 334 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ 2.82 (t, 2H), 2.92 (t, 2H), 3.77 (s, 2H), 3.80 (s, 3H), 6.80 (m, 3H), 6.98 (m, 3H), 6.08 (t, 1H), 7.22 (m, 3H), 7.32 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631401
Source datasetuspto-grants-1997_05
ORD IDord-101e2eade719414ba492ff8051d17790
Source noteuspto-grants-1997_05