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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-(Bromomethyl)-4-chlorobenzene | HCID 69329 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 2-(1H-1,2,3-benzotriazol-1-yl)-N-methoxy-N-methylacetamide | HCID 22270490 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(1H-1,2,3-Benzotriazol-1-yl)-3-(4-chlorophenyl)-N-methoxy-N-methyl-propanamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423067B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-5cd5b028df3246528087d6b0b126e15f |
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| 출처 메모 | uspto-grants-2008_09 |
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