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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1941156생성일: 2026년 10월 25일

Phenethyl bromide → 3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-one

https://huagongshe.com/reaction/1941156

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물BenzothiazoloneHCID 13625—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-oneHCID 109314680%

반응 단계

(1aB) Benzothiazolin-2-one (5.15 g, 34.1 mmol) was dissolved in dimethylformamide (100 ml) and to the solution was added 60% sodium hydride (1.36 g, 34.1 mmol) which was stirred at room temperature until generation of hydrogen gas stopped. Then β-phenylethylbromide (4.89 ml, 35.8 mmol) was added to the solution which was stirred at room temperature for 17 hours. To the reaction solution was added a saturated aqueous solution of ammonium chloride, followed by extraction with ethyl acetate. The organic layer was washed in turn with a saturated sodium bicarbonate solution and saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The crude product thus obtained was purified by subjecting it to silica gel column chromatography to give 6.49 g of 3-phenethylbenzothiazoline-2-one as a white amorphous powder form n-hexane/ethyl (4:1)-eluted fraction (yield: 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05703071
출처 데이터셋uspto-grants-1997_12
ORD IDord-4180b3f6fe5f4fb1956ba874b2beb221
출처 메모uspto-grants-1997_12