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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723798Generated: November 1, 2026

Acetophenone → HCID 10491737, compound

https://huagongshe.com/reaction/1723798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantTryptamine hydrochlorideHCID 67652—
Solvent1-ButanolHCID 263—
ProductHCID 10491737HCID 1049173756.4%

Reaction Steps

1-Methyl-1-phenyl-1,3,4,9-tetrahydrobeta-carboline was prepared by the addition of tryptamine-HCl (500 mg, 2.54 mmol), 1-butanol (12 mL), and acetophenone (1.5 mL, 13 mmol) to a 25 mL flask attached with Dean-Stark Trap. Azeotropic removal of a butanol/H2O mixture was conducted during a vigorous reflux period of 4 hours. The concentrated solution was allowed to stir near reflux for an additional 14 hours. The solution was concentrated under reduced pressure. The residue was taken up into EtOAc (70 mL), washed with sat. NaHCO3 (40 mL×3), washed with H2O (40 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material was chromatographed (SiO2 100% DCM to 5% MeOH) to provide 376 mg of 1-methyl-1-phenyl-1,3,4,9-tetrahydrobeta-carboline; 1H NMR (CDCl3) δ 7.74 (1H, br s), 7.54 (1H, d), 7.23-7.32 (6H, m), 7.09-7.21 (2H, m), 3.13 (1H, m), 2.71-2.94 (3H, m), 1.84 (3H, s); 13C NMR (CDCl3) δ 146, 138, 136, 128, 127, 127, 126, 122, 119, 118, 110, 110, 57, 40, 28, 23; TLC (SiO2, 10:1 DCM/MeOH) Rf=0.3; MS (ESI): 263 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485634B2
Source datasetuspto-grants-2009_02
ORD IDord-7c4ba74f54af446fbda8d8f0da577930
Source noteuspto-grants-2009_02