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HRID 2175778作成日:2026年10月25日

4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide → (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one

https://huagongshe.com/reaction/2175778

反応式

関与物質

役割名称HCID仕込み量
反応物4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamideHCID 86693033—
溶媒Hydrochloric AcidHCID 313—
溶媒1,4-DioxaneHCID 31275—
生成物(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—

反応手順

A solution of 4-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide (12.2 g, 38.8 mmol) dissolved in 4N HCl in dioxane (200 mL) was stirred at room temperature and monitored by TLC. After 3 days the reaction was partitioned between EtOAc (300 mL) and water (300 mL). The aqueous phase was further extracted with EtOAc (2×250 mL). The combined organic layers were then washed with water (200 mL), brine (200 mL), dried over magnesium sulfate, filtered and concentrated. The crude material was then purified via MPLC (15-30% EtOAc/Hexane) to afford (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one: 1H NMR (500 MHz; CDCl3): 7.98 (d, J=8.2 Hz, 1H), 7.56 (dd, J=1.5, 8.2 Hz, 1H), 7.45 (s, 1H), 4.71 (m, 1H), 2.94 (m, 2H), 1.55 (d, J=6.3 Hz, 3H); LC-MS: (M+1)+ 241.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09062070B2
出典データセットuspto-grants-2015_06
ORD IDord-10d94f4369b243c4a4a984d2df7137e7
出典メモuspto-grants-2015_06