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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30328생성일: 2026년 10월 24일

1-(Bromomethyl)-2-phenylbenzene → 2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanol

https://huagongshe.com/ko/reaction/30328

반응식

참여 물질

역할이름HCID투입량
반응물1-(Bromomethyl)-2-phenylbenzeneHCID 263365—
반응물(4-benzylmorpholin-2-yl)(tetrahydro-2H-pyran-4-yl)methanoneHCID 59789303—
반응물HCID 178419666HCID 178419666—
생성물2-[1,1'Biphenyl]-2-yl-1-[4-(phenylmethyl)morpholin-2-yl]-1-tetrahydro-2H-pyran-4-ylethanolHCID 58854907—
생성물HCID 178419666HCID 178419666—

반응 단계

Compound 55 is prepared from 8 (0.56 g, 1.94 mmol) and 2-phenyl benzyl magnesium bromide solution (0.25 M solution in diethyl ether, 9.31 mL, 2,33 mmol, 1.2 eq) following General Procedure 2. 2-Phenylbenzyl magnesium bromide is prepared from commercially available (Aldrich) 2-phenylbenzyl bromide following General Procedure 5. Further 2-phenyl benzyl magnesium bromide solution (1 mL) is added and the reaction left under stirring overnight. Purification by ion exchange chromatography gives 55 as an off-white foam-like solid (0.37 g, 68%). MW 457.62; C30H35NO3; LCMS. (6 minute method): m/z 458 [M+H]+, RT 3.58 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423037B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ca69a0b3786d4eeab4cf3763ad020698
출처 메모uspto-grants-2008_09