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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28211생성일: 2026년 10월 23일

m-Chloroperbenzoic acid → 3-Chlorobenzoic Acid

https://huagongshe.com/ko/reaction/28211

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물4-(3-((2-(1-Hydroxycyclohexyl)ethyl)-4-oxo-2-thiazolidinyl)propyl)benzoic acidHCID 175027—
용매ChloroformHCID 6212—
생성물3-Chlorobenzoic AcidHCID 447—

반응 단계

A mixture of 4-{3-[3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic acid (0.391 g., 1.0 mmol.), m-chloroperoxybenzoic acid (100%, 0.362 g., 2.1 mmol.), and chloroform (5 ml.) is refluxed for 30 minutes. The reaction mixture is evaporated in vacuo to give a solid residue which is applied to a silica gel column (18 g.) with chloroform. Elution with chloroform-acetic acid (25:1; v:v; 150 ml.) provides m-chlorobenzoic acid and impure material. Continued elution with the same eluant affords the title compound as a colorless viscous oil (0.273 g., 0.64 mmol., 64%), pmr (CDCl3) δ 3.75 (2H, s), 4.60 (1H, m), 7.26 (2H, d), 8.00 (2H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225609
출처 데이터셋uspto-grants-1980_09
ORD IDord-375eefff29a44514bd40b491acd8f786
출처 메모uspto-grants-1980_09