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HRID 918035作成日:2026年10月27日

2-(4-Morpholino)thiobenzothiazole → 2-(4-Morpholinyldithio)benzothiazole

https://huagongshe.com/reaction/918035

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Morpholino)thiobenzothiazoleHCID 7619—
反応物Sodium HydroxideHCID 14798—
反応物SodiumHCID 5360545—
反応物SulfurHCID 5362487—
反応物HCID 178418395HCID 178418395—
溶媒IsopropanolHCID 3776—
生成物2-(4-Morpholinyldithio)benzothiazoleHCID 723194.4%

反応条件

温度82.5 °C

反応手順

There is charged to a glass or glass-lined reactor 25.2 grams (0.1 mole) of 2-(morpholinothio)benzothiazole, 3.2 grams (0.1 mole) of sulfur, and 150 ml. of essentially anhydrous isopropyl alcohol (0.4% by weight water). The catalyst, the sodium salt of mercaptobenzothiazole, is used in amount of 0.01 mole and is formed in situ by adding 0.01 mole of solid sodium hydroxide and then 0.01 mole of 2-mercaptobenzothiazole (MBT) to the reaction mixture. The reaction mixture is then stirred and heated at refluxing temperature (about 82-83°C) for 2 hours although it is found that the reaction is essentially complete in one hour. A clear solution usually forms in from 15 to 75 minutes. The reaction mixture is cooled to 30°C. during which cooling a precipitate usually begins to form in the range of 67-74°C. Stirring and cooling is continued to 0°C. and the mixture is held at 0-10°C. for about 30 minutes after which it is filtered and the solids air dried at 25-30°C. There is obtained a yield of 94.4-95% of 2-(morpholinodithio)benzothiazole, m.p. 132°-136°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03969350
出典データセットuspto-grants-1976_07
ORD IDord-bc424d6adc3d4f82ac203c9ddd94d348
出典メモuspto-grants-1976_07