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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479609생성일: 2026년 10월 26일

Potassium Carbonate → (E)-tert-butyl 2-chloro-5-(2-cyclopropylvinyl)phenylcarbamate

https://huagongshe.com/reaction/1479609

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(E)-2-Cyclopropylethylene-1-boronic acid, pinacol esterHCID 16217940—
반응물tert-butyl N-(5-bromo-2-chlorophenyl)carbamateHCID 57840526—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물(E)-tert-butyl 2-chloro-5-(2-cyclopropylvinyl)phenylcarbamateHCID 66875036—

반응 조건

온도100 °C

반응 단계

A solution of tert-butyl 5-bromo-2-chlorophenylcarbamate (from the previous step) (1.0 eq.) and (E)-2-(2-cyclopropylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (commercially available) (1.0 eq.) in toluene (0.2 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction mixture was diluted with EtOAc and water. The two phases were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-5% EtOAc/Hexanes to give (E)-tert-butyl 2-chloro-5-(2-cyclopropylvinyl)phenylcarbamate as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09408907B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-d004518b40004f90851ea610edda2f92
출처 메모uspto-grants-2016_08