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Dimethylformamide dimethyl acetal → 4-fluoro-1H-indol-5-ol

HRID 450206
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HRID 450206 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([CH3:18])[C:10]=1[F:19])C1C=CC=CC=1.[CH3:20]OC(OC)N(C)C>[Pd]>[F:19][C:10]1[C:9]([OH:8])=[CH:14][CH:13]=[C:12]2[C:11]=1[CH:18]=[CH:20][NH:15]2
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참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 59394770HCID 59394770, 화합물

생성물 1

HCID 220305534-fluoro-1H-indol-5-ol수율 52%

시약·촉매·용매 1

HCID 23938Palladium촉매

반응 조건

온도
180 °C

실험 절차

1-Benzyloxy-2-fluoro-3-methyl-4-nitrobenzene (5 g, 19 mmol) is dissolved N,N-dimethylformamide dimethyl acetal (15 mL) and heated in a microwave reactor at 180° C. in a sealed vial for 1 hour. The solution is then concentrated under reduced pressure. The resulting residue is dissolved in THF and Pd/C (1.0 g, 10%, 0.95 mmol) is added. The mixture is stirred under a hydrogen atmosphere at room temperature for 16 h before being filtered through a pad of Celite® and concentrated. The residue is separated by FCC (EtOAc/heptane from 0 to 40%) to give 4-fluoro-1H-indol-5-ol (1.5 g, 52% yield). MS (ESI) m/z 152.1 (M+1); 1H NMR (400 MHz, DMSO-d6) δ ppm 11.02 (br. s., 1H), 8.79 (s, 1H), 7.26 (t, J=2.78 Hz, 1H), 7.00 (d, J=8.59 Hz, 1H), 6.75 (t, J=8.46 Hz, 1H), 6.34 (m, 1H).

후처리

  1. concentrationThe solution is then concentrated under reduced pressure
  2. dissolutionThe resulting residue is dissolved in THF
  3. filtrationbefore being filtered through a pad of Celite®
  4. concentrationconcentrated
  5. customThe residue is separated by FCC (EtOAc/heptane from 0 to 40%)

출처 및 근거

ORD 기록
ord-ede82a320455435da464fb1fec37f617
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08486954B2

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