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HRID 724744作成日:2026年10月26日

Levodopa → 5,6-Dihydroxyindole

https://huagongshe.com/reaction/724744

反応式

関与物質

役割名称HCID仕込み量
反応物LevodopaHCID 6047—
反応物DopachromeHCID 119399—
反応物Sodium BicarbonateHCID 516892—
反応物DihydroxymethylindoleHCID 22747466—
反応物3-Hydroxy-N-methyl-L-tyrosineHCID 23620856—
触媒Zinc AcetateHCID 11192—
触媒HCID 178511488HCID 178511488—
生成物5,6-DihydroxyindoleHCID 114683—

反応手順

The Bu'Lock et al article discloses oxidation often 2-3', 4'-dihydroxyphenylethyl amine derivatives, including dopa. For methyl dopa (described at page 2251), a 4.735×10-2M concentration of methyl dopa was reacted with a 0.1974M concentration of potassium ferricyanide, in the presence of sodium bicarbonate buffer at a 0.238M concentration. After 10 minutes 8 cc of a 20% zinc acetate solution was added to effect rearrangement of the dopachrome to the dihydroxymethylindole. The article indicates that a similar procedure was used for dopa. The reported 5,6-dihydroxyindole yield of one experiment, after purification, was 30%. However, the Bu'Lock article states that this yield could not be repeated. According to the article the solid light-brown residue obtained in subsequent experiments appeared to be polymeric. At page 2249 Bu'Lock et al hypothesized that their inability to repeat the sole successful experiment was attributable to the diluteness of the reaction medium. This later article by Bu'Lock et al supplements their prior article in Nature, 166:1036-7 (1950), which reported "an excellent yield" of 5,6-dihydroxyindole, and essentially negates their original findings.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05704949
出典データセットuspto-grants-1998_01
ORD IDord-9aefcd62bd054c628367e326fd40f2b9
出典メモuspto-grants-1998_01