돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1919898생성일: 2026년 10월 27일

Methyl 4-(bromomethyl)benzoate → Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoate

https://huagongshe.com/reaction/1919898

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-(bromomethyl)benzoateHCID 256687—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물tert-Butyl ((tert-butoxycarbonyl)amino)acetateHCID 4097102—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoateHCID 57611911—

반응 조건

온도-78 °C

반응 단계

Tert-butyl[(tert-butoxycarbonyl)amino]acetate (1.01 g, 4.37 mmol) was dissolved in THF (10 mL) and cooled to −78° C. LiHMDS (6.5 mL, 1M solution in THF) was slowly added and allowed to stir for 30 minutes. Methyl 4-(bromomethyl)benzoate (1.98 g, 8.64 mmol) in THF (6 mL) was added to the mixture and allowed to stir overnight, slowly warming to room temperature. The reaction was diluted with ethyl acetate and quenched with saturated ammonium chloride. The aqueous layer was extracted three times with ethyl acetate. The combined organic layer was dried over sodium sulfate, filtered, and concentrated. The resulting residue was purified by column chromatography. MS: cal'd 379 (MH+), exp 402 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08168658B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-fd8c5cc610c84a5b9d787fb783e8e6d1
출처 메모uspto-grants-2012_05