돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250490생성일: 2026년 10월 26일

Hydrochloric Acid → 5-Cyclohexylsulfanyl-isoindole-1,3-dione

https://huagongshe.com/reaction/250490

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-NitrophthalimideHCID 6969—
반응물Potassium CarbonateHCID 11430—
반응물CyclohexanethiolHCID 15290—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물5-Cyclohexylsulfanyl-isoindole-1,3-dioneHCID 66712998114.7%

반응 단계

A mixture of 5-nitro-isoindole-1,3-dione (10.0 g), cyclohexanethiol (9.1 g) and potassium carbonate (18.7 g) in acetone (260 ml) was heated to reflux overnight. After cooling, the mixture was diluted with water (250 ml) and then acidified by 6 N HCl to pH=4. Precipitate was collected and dried in vacuo to give the intermediate 5-cyclohexylsulfanyl-isoindole-1,3-dione (15.6 g). This intermediate was dissolved in acetone (170 ml) and to the mixture was added bromo ethylacetate (10.6 g) and potassium carbonate (23.8 g). The mixture was refluxed overnight. After cooling, reaction mixture was filtered and rinsed with ethyl acetate. Filtrate was concentrated and purified by silica gel chromatography (10%-50% ethyl acetate in methylene chloride) to give the title compound (13.1 g). 1H NMR (200 MHz, CDCl3) δ 7.73 (m, 2H), 7.56 (dd, J=7.8, 1.6 Hz, 1H), 4.40 (s, 2H), 4.21 (q, J=7.0 Hz, 2H), 3.37 (m, 1H), 2.07-1.28 (m, 13H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863292B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-8ac5c61566df40678a244d34121bd897
출처 메모uspto-grants-2011_01