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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1105583생성일: 2026년 10월 26일

4-(Trifluoromethyl)benzohydrazide → S-propyl O-[2-(4-trifluoromethylbenzoylhydrazonomethyl)phenyl] ethylthiophosphonate

https://huagongshe.com/reaction/1105583

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzohydrazideHCID 520662—
반응물S-Propyl O-(2-Formylphenyl) EthylthiophosphonateHCID 57213049—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물S-propyl O-[2-(4-trifluoromethylbenzoylhydrazonomethyl)phenyl] ethylthiophosphonateHCID 86738191—

반응 단계

A solution of S-propyl O-(2-formylphenyl) ethylthiophosphonate (0.02 mole) in methanol (50 ml) and 4-trifluoromethylbenzoylhydrazine (0.02 mole) are charged into a glass reaction vessel and the mixture is stirred at room temperature for a period of about 12 hours. After this time the reaction mixture is stripped of methanol under vacuum and the residue is dissolved in methylene chloride (100 ml) and the resulting solution is washed with water (75 ml) with aqueous sodium hydroxide (75 ml; 0.1 N) and again with water (75 ml). The washed solution is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent to yield the desired product S-propyl O-[2-(4-trifluoromethylbenzoylhydrazonomethyl)phenyl] ethylthiophosphonate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04309422
출처 데이터셋uspto-grants-1982_01
ORD IDord-4b53bb03a06c4439a31527c482025fc6
출처 메모uspto-grants-1982_01