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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1988796생성일: 2026년 10월 27일

Pyridine → {[1-(naphthalen-1-yl)-1H-tetrazol-5-yl]sulfanyl}acetic acid

https://huagongshe.com/reaction/1988796

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Methyl bromoacetateHCID 60984—
반응물1,2-Dihydro-1-naphthyl-5H-tetrazole-5-thioneHCID 2731701—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물{[1-(naphthalen-1-yl)-1H-tetrazol-5-yl]sulfanyl}acetic acidHCID 2907025992.3%

반응 단계

Pyridine (0.83 mL, 10.3 mmol) and 1,2-dihydro-1-(1-naphthalenyl)-5H-tetrazole-5-thione (2.14 g, 9.38 mmol) were added to a solution of methyl 2-bromoacetate (977 μL, 10.3 mmol) in DMSO (50 mL). The resulting light yellow solution was stirred at room temperature for 2 h. The reaction mixture was then diluted with EtOAc (300 ml) and was successively washed with water (2×250 ml) and brine (100 ml), dried (MgSO4), filtered and concentrated under reduced pressure. The crude ester was dissolved in THF and aqueous 1 N NaOH solution was added. The solution was stirred at room temperature for 30 min. The THF was evaporated under reduced pressure and the residue was dissolved in aqueous 1 N NaOH solution. The solution was slowly acidified to pH 2 at 0° C. with aqueous 1 N HCl solution. The suspension was filtered and the resulting solid was rinsed with water and dried under reduced pressure to give the title compound (2.48 g, 92% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07642277B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-35c8c0f67b7241feb41bc2376819755a
출처 메모uspto-grants-2010_01