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

HRID 2173416

반응식

HRID 2173416 반응식
[Br:1][C:2]1[CH:14]=[CH:13][C:5]([C:6](N(CC)CC)=[O:7])=[C:4]([CH2:15][C@H:16]([OH:18])[CH3:17])[CH:3]=1>Cl.O1CCOCC1>[Br:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:13][CH:14]=1)[C:6](=[O:7])[O:18][C@H:16]([CH3:17])[CH2:15]2

참가 물질

4

반응물 1

HCID 866930334-bromo-N,N-diethyl-2-[(2R)-2-hydroxypropyl]benzamide

생성물 1

HCID 71270763(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

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.

후처리

  1. customAfter 3 days the reaction was partitioned between EtOAc (300 mL) and water (300 mL)
  2. extractionThe aqueous phase was further extracted with EtOAc (2×250 mL)
  3. washThe combined organic layers were then washed with water (200 mL), brine (200 mL)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude material was then purified via MPLC (15-30% EtOAc/Hexane)

출처 및 근거

ORD 기록
ord-3c04e482e78148dea07a0d263a539a6a
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09056859B2

연결된 노트

불러오는 중…