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HRID 52261作成日:2026年10月24日

Hydrochloric Acid → (R)-8-Bromo-3-(N-isopropylamino)-5-methoxy-3,4-dihydro-2H-1-benzopyran

https://huagongshe.com/ja/reaction/52261

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BromineHCID 24408—
反応物Sodium AcetateHCID 517045—
反応物(R)-3-(N-Isopropylamino)-5-methoxychromanHCID 10489181—
溶媒Acetic AcidHCID 176—
溶媒Diethyl EtherHCID 3283—
生成物(R)-8-Bromo-3-(N-isopropylamino)-5-methoxy-3,4-dihydro-2H-1-benzopyranHCID 5402930562%

反応手順

(R)-3-(N-Isopropylamino)-5-methoxy-3,4-dihydro-2H-1-benzopyran (4.02 g, 18.2 mmol) and anhydrous sodium acetate were dissolved in acetic acid (80 mL). To the stirred mixture was bromine (0.93 mL, 18.2 mmol) dissolved in acetic acid (40 mL) added dropwise under 1.5 h. The solvent was removed in vacuo, taken into a 2M NaOH solution and extracted twice with diethyl ether. The combined ether portions were treated with brine, dried (Na2SO4), filtered, and the solvent was removed in vacuo to give the crude residue. The hydrochloride salt was made by dissolving the pure base in diethyl ether and adding an excess of an ethereal HCl solution to give a white solid. The salt was recrystallized twice from ethanol/diethyl ether to give 3.8 g (62% yield) Mp: 257°-8° C. [α]21D =-97.7° (C=0.1 CHCl3). The free base was made from the hydrochloride salt to give an oil. GC-MS (70 eV) M=301 (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616610
出典データセットuspto-grants-1997_04
ORD IDord-26091e83879c49e796630f835fb52b94
出典メモuspto-grants-1997_04