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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30245생성일: 2026년 10월 24일

4,5-Dibromothiophene-2-carbaldehyde → cis-3-(4,5-Dibromo-thiophen-2-yl)-acrylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/30245

반응식

참여 물질

역할이름HCID투입량
반응물4,5-Dibromothiophene-2-carbaldehydeHCID 813164—
반응물Tert-butyl (diphenoxyphosphoryl)acetateHCID 10689048—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물cis-3-(4,5-Dibromo-thiophen-2-yl)-acrylic acid tert-butyl esterHCID 67205492—

반응 조건

온도-78 °C

반응 단계

(Diphenoxy-phosphoryl)-acetic acid tert-butyl ester (8.49 g, 24.4 mmol) was dissolved in THF (519 ml) and cooled to −78° C. followed by the addition of triton B (13.3 ml, 40% by wt. in MeOH). After 15 minutes a solution of 4,5-Dibromo-thiophene-2-carbaldehyde (7.0 g, 25.9 mmol) in THF (20 ml) was added and the reaction was stirred for 1 hour. Next, the reaction mixture was quenched with sat. NH4Cl (250 ml), diluted with H2O (500 ml), and extracted with EtOAc (2×300 ml). The organic layers were washed with water (2×200 ml), brine (100 ml), and dried (MgSO4). The crude was passed through a plug of silica gel with EtOAc providing the desired product 9.2 g (96%) as a 4:1 mixture of cis:trans. MS calculated for C10H12BrNS−H 367, observed M-tBu 309, 311, 313.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-295c8f725dc14dd58e85687443b962aa
출처 메모uspto-grants-2008_09