Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10899생성일: 2026년 10월 23일
Toluene-p-sulphonic anhydride → Allyl 2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
https://huagongshe.com/ko/reaction/10899
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Toluene-p-sulphonic anhydride | HCID 77773 | — |
| 반응물 | Allyl 3-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate | HCID 21982185 | — |
| 용매 | Propan-2-one--water (1/1) | HCID 18366337 | — |
| 생성물 | Allyl 2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate | HCID 21982199 | — |
반응 단계
Allyl 3-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate (331 mg, 0.91 mmol) was dissolved in a a solvent mixture of acetone/water (v/v=5/1), and catalyst amount of p-toluenesulfonic acid anhydride was added to the obtained solution. The resulting mixture was refluxed at 80° C. for 18 hours. After the reaction was completed, the reaction mixture was washed with water, and then acetone was removed by distilling under a reduced pressure. The residue was extracted with dichloromethane. The combined organic layer was dried with anhydrous sulfate and distilled under a reduced pressure. The desired product was obtained (131.2 mg, 31%) by performing column chromatography (eluent: n-hexane/ethyl acetate=2/1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094908B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-dbb505f7b1a54d5491bd553456441248 |
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| 출처 메모 | uspto-grants-2006_08 |
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