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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4947생성일: 2026년 10월 23일

3,5-Dimethyl-4-hydroxybenzonitrile → Win 58768

https://huagongshe.com/ko/reaction/4947

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dimethyl-4-hydroxybenzonitrileHCID 20176—
반응물Win 58768HCID 148372—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물6-n-Propyl-3-(4-hydroxy-1-piperidinyl)pyridazineHCID 19797304—
생성물Win 58768HCID 148372—
생성물(3,5-dimethyl-4-hydroxyphenyl)-2H-tetrazoleHCID 86747187—

반응 단계

2-Methyl-5-((3,5-dimethyl-4-hydroxyphenyl)-2H-tetrazole (Formula III: R2 =R3 =R4 =CH3) was prepared according to the procedure of Example 1b starting with 2,6-dimethyl-4-cyanophenol. 4.5 Mmol of 6-methyl-3-(4-hydroxyl-1-piperidinyl)pyridazine (Formula IV: R1 =methyl, Y=CH2), 1.14 g DEAD, 6.8 mmol TPP, 5 mmol of 2-methyl-5-(3,5-dimethyl-4-hydroxyphenyl)-2H-tetrazole (Formula III: R2 =R3 =R4 =CH3) were reacted as described in Example 1c. Recrystallization from ethyl acetate afforded a 71.9% yield of the compound of Formula I (R1 =R2 =R3 =R4 =methyl, Y=CH2) m.p. 183°-184° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242924
출처 데이터셋uspto-grants-1993_09
ORD IDord-497fa056f7bb46efa7e51c283e600987
출처 메모uspto-grants-1993_09