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Triethyl phosphite → HCID 90403989, 화합물

HRID 1468960
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HRID 1468960 반응식
[Br:1][C:2]1[C:3]([F:12])=[CH:4][C:5]2[C:6]([CH:11]=1)=[N+:7]([O-])[O:8][N:9]=2.C(OP(OCC)OCC)C>C(O)C>[Br:1][C:2]1[C:3]([F:12])=[CH:4][C:5]2=[N:9][O:8][N:7]=[C:6]2[CH:11]=1
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참가 물질

4

반응물 2

HCID 31215Triethyl phosphiteHCID 90403441HCID 90403441, 화합물

생성물 1

HCID 90403989HCID 90403989, 화합물수율 73%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
45 °C

실험 절차

6-bromo-5-fluorobenzo[c][1,2,5]oxadiazole 1-oxide (3.2 g, 14 mmol) was stirred in 30 mL ethanol, treated with triethylphosphite (3.4 g, 21 mmol) and heated to 45° C. After 90 min, the mixture was cooled and the volatiles were removed by rotary evaporation. The crude product was chromatographed on silica gel with a 0-10% ethyl acetate-hexane gradient to give the title compound as tan crystals (2.2 g, 73%): mp 59-61° C.; 1H NMR (400 MHz, CDCl3) δ 8.23 (dt, J=2.8, 1.4 Hz, 1H), 7.53 (m, 1H); 19F NMR (376 MHz, CDCl3) δ −96.99; EIMS m/z 216.

후처리

  1. temperaturethe mixture was cooled
  2. customthe volatiles were removed by rotary evaporation
  3. customThe crude product was chromatographed on silica gel with a 0-10% ethyl acetate-hexane gradient

출처 및 근거

ORD 기록
ord-1f45d5833d104f6fb1de8f063bd7fb3b
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006250B2

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