돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37728생성일: 2026년 10월 24일

Methanol → methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate

https://huagongshe.com/ko/reaction/37728

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
반응물Methyl 7-(4-fluorophenyl)-7-oxoheptanoateHCID 19936161—
용매TetrahydrofuranHCID 8028—
생성물methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoateHCID 1056289298.4%

반응 단계

To a solution of (R)-3,3-diphenyl-1-methyltetrahydro-1H,3H-pyrrolo[1,2-c] [1,3,2]oxazaborole (1.1 g) in tetrahydrofuran (20 ml) was added at 0° C. 1M tetrahydrofuran solution of boranetetrahydrofuran complex (4 ml). To this solution were added dropwise a solution of methyl 7-(4-fluorophenyl)-7-oxoheptanoate (10.0 g, 39.6 mmol) in tetrahydrofuran (20 ml) and 1M tetrahydrofuran solution of boranetetrahydrofuran complex (20 ml), simultaneously, taking 25 minutes. The mixture was stirred for 30 minutes at the same temperature range, to which was added methanol (20 ml), followed by stirring for 30 minutes at room temperature. The solvent was distilled off under reduced pressure, and the residue was subjected to a silica gel column chromatography to give methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate (9.91 g). Physico-chemical properties and spectral data of this product are shown in [Table 7]. Likewise, Compound 1-2 was prepared.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420363
출처 데이터셋uspto-grants-1995_05
ORD IDord-5fdb7b29cd3c48a78d22172e09f3d335
출처 메모uspto-grants-1995_05