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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52261생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/52261

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BromineHCID 24408—
반응물Sodium AcetateHCID 517045—
반응물(R)-3-(N-Isopropylamino)-5-methoxychromanHCID 10489181—
용매Acetic AcidHCID 176—
용매Diethyl EtherHCID 3283—
생성물(R)-8-Bromo-3-(N-isopropylamino)-5-methoxy-3,4-dihydro-2H-1-benzopyranHCID 5402930562%

반응 단계

(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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616610
출처 데이터셋uspto-grants-1997_04
ORD IDord-26091e83879c49e796630f835fb52b94
출처 메모uspto-grants-1997_04