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(RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzaldehyde → 2-cyclopropyl-7,8-dimethoxy-2H-chromene-5-carbaldehyde

HRID 964970
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HRID 964970 반응식
[CH:1]1([CH:4]([O:7][C:8]2[CH:9]=[C:10]([CH:13]=[C:14]([O:18][CH3:19])[C:15]=2[O:16][CH3:17])[CH:11]=[O:12])[C:5]#[CH:6])[CH2:3][CH2:2]1>C(N(CC)C1C=CC=CC=1)C>[CH:1]1([CH:4]2[CH:5]=[CH:6][C:9]3=[C:10]([CH:11]=[O:12])[CH:13]=[C:14]([O:18][CH3:19])[C:15]([O:16][CH3:17])=[C:8]3[O:7]2)[CH2:3][CH2:2]1
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참가 물질

3

반응물 1

HCID 19074980(RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzaldehyde

생성물 1

HCID 115506702-cyclopropyl-7,8-dimethoxy-2H-chromene-5-carbaldehyde

시약·촉매·용매 1

HCID 7061N,N-Diethylaniline용매

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온도
200 °C

실험 절차

2.4 g of (RS)-3-(1-cyclopropyl-prop-2-ynyloxy)-4,5-dimethoxy-benzaldehyde were dissolved in 20 ml of N,N-diethyl-aniline, heated to 200° C. under argon and stirred at 200° C. for a further 1 hr. The solvent was distilled off at 90° C./1 mbar and the residue was extracted: 2×100 ml of diethyl ether, 2×100 ml of 1N HCl, 2×100 ml of saturated NaCl. The crude product was purified by two-fold silica gel chromatography with dichloromethane and, respectively, ethyl acetate/hexane 5:1. (RS)-2-Cyclopropyl-7,8-dimethoxy-2H-1-benzopyran-5-carbaldehyde was obtained as a brown oil (HPLC 96%).

후처리

  1. distillationThe solvent was distilled off at 90° C./1 mbar
  2. extractionthe residue was extracted
  3. customThe crude product was purified by two-fold silica gel chromatography with dichloromethane

출처 및 근거

ORD 기록
ord-b8cc833b29334574ad08fd6bbbabde0b
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773446

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