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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034256Generated: November 1, 2026

Acetic Anhydride → HCID 18328986, compound

https://huagongshe.com/reaction/1034256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2,3,4,9-Tetrahydro-6-methoxy-1-methyl-1H-pyrido(3,4-b)indoleHCID 71028—
CatalystAmmonium HydroxideHCID 14923—
SolventEthyl AcetateHCID 8857—
ProductHCID 18328986HCID 18328986—

Reaction Steps

To a solution of 700 mg (3.24 mmol) 1-methyl-6-methoxy-1,2,3,4-tetrahydro-β-carboline, and 5 drops NH4OH in ethyl acetate was added 0.4 mL (3.88 mmol) acetic anhydride under N2 gas. The reaction was stirred for 20 min. and then washed with water. The organic layer collected was dried over MgSO4, filtered, and concentrated in vacuo to a dark oil. The oil was dissolved in methanol and chromatographed on reverse phase C-18 using methanol and water. The product was collected and concentrated to a white solid, which showed characteristic peaks: NMR (CDCl3) δ: 1.45 ppm (d, 3H), 2.25 ppm (s, 3H), 3.85 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05314908
Source datasetuspto-grants-1994_05
ORD IDord-36e5f3b52127447b84cfc08d4bcd774f
Source noteuspto-grants-1994_05