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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1753720생성일: 2026년 10월 24일

Oxalyl chloride → 2-methoxy-3-(methylsulfanyl)-N-(1-methyl-1H-tetrazol-5-yl)-4-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/1753720

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물1-methyl-1H-tetrazol-5-amineHCID 138492—
반응물2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoic acidHCID 66957907—
용매PyridineHCID 1049—
생성물2-methoxy-3-(methylsulfanyl)-N-(1-methyl-1H-tetrazol-5-yl)-4-(trifluoromethyl)benzamideHCID 8976879246.6%

반응 단계

1.45 g (98% by weight; 14.3 mmol) of 5-amino-1-methyl-1H-tetrazole were added to 3.00 g (11.3 mmol) of 2-methoxy-3-(methylsulfanyl)-4-(trifluoromethyl)benzoic acid in 30 ml of dry pyridine. 2.00 g (15.8 mmol) of oxalyl chloride were then added, and the mixture was subsequently stirred at room temperature (RT) for three days. Another 500 mg (3.94 mmol) of oxalyl chloride were then added, and the mixture was subsequently stirred at RT for 16 h. For work-up, the contents were substantially freed from the solvent on a rotary evaporator. The residue was stirred with dichloromethane and a saturated solution of sodium bicarbonate. The organic phases were then separated and the organic phase was freed from the solvent on a rotary evaporator. The residue was purified chromatographically, which gave 1.83 g of clean product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09167819B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-6e42f933ffe44b92a03fe1941df17cc5
출처 메모uspto-grants-2015_10