돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2286801생성일: 2026년 10월 26일

Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)- → alpha-Cyano-m-phenoxybenzyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoate

https://huagongshe.com/reaction/2286801

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)-HCID 93218—
반응물(3-Fluorophenyl)acetaldehydeHCID 15811999—
반응물4-(3-Fluorophenyl)-2-isopropyl-3-butenoic acidHCID 53669376—
반응물Ethyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoateHCID 54533755—
반응물KOH MeOH WaterHCID 86591755—
생성물alpha-Cyano-m-phenoxybenzyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoateHCID 53932607—

반응 단계

3-Fluorophenylacetaldehyde is converted into ethyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoate using the reaction of Example 9. The ester is hydrolyzed using KOH/MeOH/H2O to 4-(3-fluorophenyl)-2-isopropyl-3-butenoic acid, which is converted to the acid chloride and reacted with α-cyano-m-phenoxybenzyl alcohol to yield α-cyano-m-phenoxybenzyl 4-(3-fluorophenyl)-2-isopropyl-3-butenoate, MS m/e 429 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04267359
출처 데이터셋uspto-grants-1981_05
ORD IDord-f7f970fae2fa4bbf93036adf29981be6
출처 메모uspto-grants-1981_05