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HRID 918035생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/918035

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Morpholino)thiobenzothiazoleHCID 7619—
반응물Sodium HydroxideHCID 14798—
반응물SodiumHCID 5360545—
반응물SulfurHCID 5362487—
반응물HCID 178418395HCID 178418395—
용매IsopropanolHCID 3776—
생성물2-(4-Morpholinyldithio)benzothiazoleHCID 723194.4%

반응 조건

온도82.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03969350
출처 데이터셋uspto-grants-1976_07
ORD IDord-bc424d6adc3d4f82ac203c9ddd94d348
출처 메모uspto-grants-1976_07