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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276270생성일: 2026년 10월 24일

3-Bromo-2-methyl-1-propene → N-(tert-butoxycarbonyl)-N-(2-methylprop-2-enyl)glycine tert-butyl ester

https://huagongshe.com/ko/reaction/276270

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-2-methyl-1-propeneHCID 357785—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물tert-Butyl ((tert-butoxycarbonyl)amino)acetateHCID 4097102—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(tert-butoxycarbonyl)-N-(2-methylprop-2-enyl)glycine tert-butyl esterHCID 1831604382.1%

반응 단계

To a solution of N-(tert-butoxycarbonyl)glycine tert-butyl ester (3.97 g, 17.2 mmol) in DMF (70 mL) at 0° C. was added sodium hexamethyldisilazide (3.78 g, 20.6 mmol) and the resulting mixture was stirred for 25 min., then allowed to warm to room temp. The resulting solution was treated with 3-bromo-2-methylpropene (2.60 mL, 25.7 mmol), stirred at room temp. for 10 min., and diluted with EtOAc (300 mL). The EtOAc solution was sequentially washed with water (4×500 mL) and a saturated NaCl solution (4×500 mL), dried (MgSO4), and concentrated under reduced pressure to afford N-(tert-butoxycarbonyl)-N-(2-methylprop-2-enyl)glycine tert-butyl ester (4.03 g, 82%): TLC (10% EtOAc/hex) Rf0.51.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06353006B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-e09cb2a2c9324b9389781078417047af
출처 메모uspto-grants-2002_03