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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2418921생성일: 2026년 10월 25일

Benzothiazole → 3-Benzothiazol-2-yl-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2418921

반응식

참여 물질

역할이름HCID투입량
반응물BenzothiazoleHCID 7222—
반응물Tert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
시약Hydrogen PeroxideHCID 784—
시약Sulfuric AcidHCID 1118—
촉매CID 516917HCID 516917—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물3-Benzothiazol-2-yl-azetidine-1-carboxylic acid tert-butyl esterHCID 4423981815%

반응 조건

온도25 °C

반응 단계

H2O2 (30% in H2O; 0.31 mL, 3.0 mmol) was added to a stirred solution of benzothiazole 1f (108 μL, 1.0 mmol), concentrated H2SO4 (53 μL, 1.0 mmol), 1-Boc-3-(iodo)azetidine (849 mg, 3.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) in DMSO (10 mL) at room temperature. After 1-2 min a further portion of iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added and the mixture was stirred at room temperature for 30 min. Further H2O2 (0.31 mL, 3.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added, and the mixture was stirred for overnight, then poured into a 0.2 M solution of NaOH (30 mL) and EtOAc (50 mL). The aqueous and organic layers were partitioned and the organic layer was dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by preparative thin-layer chromatography using EtOAc / hexanes (1:4) as eluent to give a mixture of recovered benzothiazole 1f and 1-BOC-3-(iodo)azetidine, and the desired product 3e (45 mg, 15%)

출처 및 근거

DOI10.1021/jo9010624
출처 데이터셋Minisci dataset from Roche
ORD IDord-af650d531fba4b5fa8017430d4872dcc
출처 메모Minisci dataset from Roche