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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357644생성일: 2026년 10월 24일

Acetic Acid → Tert-butyl 4-hydroxy-4-(4-methoxycarbonyl-6-nitrophenyl)-2-butynoate

https://huagongshe.com/ko/reaction/357644

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물tert-Butyl propiolateHCID 543038—
반응물Lithium diisopropylamideHCID 2724682—
반응물Methyl 4-formyl-3-nitrobenzoateHCID 3457222—
반응물Tetrahydrofuran heptane ethylbenzolHCID 22742125—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-hydroxy-4-(4-methoxycarbonyl-6-nitrophenyl)-2-butynoateHCID 18937575106.2%

반응 단계

To a solution of tert-butyl propiolate (3.54 ml, 25.81 mmole) in tetrahydrofuran (60 ml) was added at -70° C. under the argon atmosphere a solution of 2.0M lithium diisopropylamide in a heptane-tetrahydrofuran-ethylbenzene mixture (13.0 ml, 26 mmole), and the mixture was stirred for 30 minutes. The reaction mixture was then added to a solution of 4-methoxycarbonyl-2-nitrobenzaldehyde (4.5 g, 21.5 mmole) in tetrahydrofuran (100 ml), and the mixture was further stirred at -75° C. for 5 minutes. After a solution of acetic acid (3.2 ml, 53.3 mmole) in tetrahydrofuran (10 ml) and water were added, the reaction mixture was extracted with ethyl acetate (400 ml). The organic layer was washed with dilute hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous saline in this sequence. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure to give the crude product of tert-butyl 4-hydroxy-4-(4-methoxycarbonyl-6-nitrophenyl)-2-butynoate as a brown oil (7.655 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840895
출처 데이터셋uspto-grants-1998_11
ORD IDord-152cc7b5fab546ad89babf657ef4fcae
출처 메모uspto-grants-1998_11