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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1656124생성일: 2026년 10월 26일

1,3,3-Trimethyl-2-methyleneindoline → 8-methacryloxymethyl-6-nitro-1',3',3'-trimethylspiro[2H-1-benzothiopyran-2,2'-indoline]

https://huagongshe.com/reaction/1656124

반응식

참여 물질

역할이름HCID투입량
반응물1,3,3-Trimethyl-2-methyleneindolineHCID 8351—
반응물3-Methacryloxymethyl-5-nitrothiosalicylaldehydeHCID 10945876—
용매Methyl Ethyl KetoneHCID 6569—
생성물8-methacryloxymethyl-6-nitro-1',3',3'-trimethylspiro[2H-1-benzothiopyran-2,2'-indoline]HCID 1087379372.7%

반응 단계

In 120 ml of 2-butanone were dissolved 14.1 g of 3-methacryloxymethyl-5-nitrothiosalicylaldehyde and 8.7 g of 2-methylene-1,3,3-trimethylindoline, and the solution was heated under reflux for 20 hours in a nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure, and the residue was purified by a silica gel column, giving 15.9 g of 8-methacryloxymethyl-6-nitro-1',3',3'-trimethylspiro[2H-1-benzothiopyran-2,2'-indoline] in the form of pale yellow crystals (yield 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05252742
출처 데이터셋uspto-grants-1993_10
ORD IDord-20d82bc80d3c429dbbe221a63ce11a2d
출처 메모uspto-grants-1993_10