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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 923456생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → tert-butyl {2-[(1Z)-prop-1-en-1-yl]benzyl}carbamate

https://huagongshe.com/reaction/923456

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물(Z)-Prop-1-en-1-ylboronic acidHCID 5355539—
반응물2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl {2-[(1Z)-prop-1-en-1-yl]benzyl}carbamateHCID 118318066648.7%

반응 단계

A mixed liquid of 1.50 g of tert-butyl(2-bromobenzyl)carbamate, 3.90 g of tripotassium phosphate, 348 mg of dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine, 195 mg of tris(dibenzylideneacetone)dipalladium(0), 905 mg of (1Z)-prop-1-en-1-yl boronic acid, 30 ml of 1,4-dioxane, and 7.5 ml of water was stirred at 90° C. for 15 hours. The reaction mixture was left to be cooled to room temperature and then filtrated over Celite. The filtrate was concentrated under reduced pressure, and then to the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and then dried over anhydrous magnesium sulfate and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography to obtain 1.36 g of tert-butyl {2-[(1Z)-prop-1-en-1-yl]benzyl}carbamate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278968B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ec9a003cbe024598972d82f1b2c6d7b6
출처 메모uspto-grants-2016_03