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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30385생성일: 2026년 10월 24일

1-(Bromomethyl)-4-chlorobenzene → 2-(1H-1,2,3-Benzotriazol-1-yl)-3-(4-chlorophenyl)-N-methoxy-N-methyl-propanamide

https://huagongshe.com/ko/reaction/30385

반응식

참여 물질

역할이름HCID투입량
반응물1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-(1H-1,2,3-benzotriazol-1-yl)-N-methoxy-N-methylacetamideHCID 22270490—
용매TetrahydrofuranHCID 8028—
생성물2-(1H-1,2,3-Benzotriazol-1-yl)-3-(4-chlorophenyl)-N-methoxy-N-methyl-propanamideHCID 22270633—

반응 단계

To a solution of 2.0 g (9 mmol) of 2-(1H-1,2,3-benzotriazol-1-yl)-N-methoxy-N-methylacetamide in 15 mL anhydrous THF at −78° C., 10 mL (10 mmol) of 1M lithium bis(trimethylsilyl)amide was added dropwise. After stirring for 25 min, a solution of 2.06 g (10 mmol) of 4-chlorobenzyl bromide in 2 mL anhydrous THF was added. The resulting reaction mixture was allowed to warm to RT and stirred for 6 h. This reaction was quenched, diluted with 75 mL EtOAc and washed 3 times with 10 mL each of brine, After drying the organic phase solvent removal afforded a crude product which was purified on silica gel using 40% EtOAc in hexane as solvent to afford the desired product as a solid. 1H NMR: (CDCl3): δ 3.2 (s, 3H), 3.34 (s, 3H), 3.52 (m, 1H), 3.7 (m, 1H), 6.32 (t, 1H), 6.9-8.2 (m, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423067B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5cd5b028df3246528087d6b0b126e15f
출처 메모uspto-grants-2008_09