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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2173417생성일: 2026년 10월 27일

Dimethylformamide → (3R)-6-(1,3-dioxolan-2-ylmethyl)-3-methyl-3,4-dihydro-1H-isochromen-1-one

https://huagongshe.com/reaction/2173417

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—
반응물HCID 178419777HCID 178419777—
촉매palladium(II) acetateHCID 167845—
용매Ethyl AcetateHCID 8857—
생성물(3R)-6-(1,3-dioxolan-2-ylmethyl)-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 86693034—

반응 조건

온도110 °C

반응 단계

A sealed tube was charged with aryl bromide, palladium(II) acetate (0.028 g, 0.124 mmol) and tri-t-butylphosphine-BF4 complex (0.072 g, 0.249 mmol) and sealed. The tube was evacuated and refilled with nitrogen before DMF (12.44 ml) and (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one (0.75 g, 3.11 mmol) were added followed by bromo(1,3-dioxolan-2-ylmethyl)zinc (6.22 ml, 3.11 mmol). The tube was heated to 110° C. in the microwave for 75 minutes, after which it was cooled, diluted with EtOAc, filtered, concentrated and purified via MPLC (20-50% E/H) to afford (3R)-6-(1,3-dioxolan-2-ylmethyl)-3-methyl-3,4-dihydro-1H-isochromen-1-one. 1H NMR (500 MHz; CDCl3): 8.04 (d, J=7.8 Hz, 1H), 7.32 (d, J=8.0 Hz, 1H), 7.17 (s, 1H), 5.11 (1, J=4.7 Hz, 1H), 4.68 (m, 1H), 3.96 (m, 2H), 3.88 (m, 2H), 3.03 (d, J=4.9 Hz, 2H), 2.93 (m, 2H), 1.54 (d, J=6.4 Hz, 3H); LC-MS (IE, m/z): 249 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09056859B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-b04b9e2987ec4a5283f269e3fb281d1e
출처 메모uspto-grants-2015_06