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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253294Generated: October 31, 2026

Oxygen → HCID 14156204, compound

https://huagongshe.com/reaction/1253294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantTolueneHCID 1140—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant7-Chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-oneHCID 14156194—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14156204HCID 14156204—

Reaction Steps

Oxygen was bubbled through a solution of 7-chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-one (7.0 g, 19.46 mmole) in 100 ml of dry tetrahydrofuran at 0° C. while a 0.67M solution of potassium hexamethyldisilazide in toluene (87.64 ml, 58.76 mmole) was added dropwise over 15 minutes. The reaction was continued for 1 hour with the continued bubbling of oxygen at 0° C. The reaction was quenched with 75 ml of a 5% solution of potassium bisulfate, followed by the addition of solid sodium sulfite and 10 ml of methanol. The reaction was stirred for 30 minutes and extracted twice with ethyl acetate. The combined organic layers were washed with 1N hydrochloric acid, saturated sodium bicarbonate, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue was recrystallized from isopropyl alcohol to yield 4.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748239
Source datasetuspto-grants-1988_05
ORD IDord-ade2b1092e2c403da413db7c00fe8787
Source noteuspto-grants-1988_05