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Phosphorus oxychloride → 7-Chloro-2-(trimethylsilyl)furo[3,2-b]pyridine

HRID 1042853
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HRID 1042853 반응식
[CH3:1][Si:2]([CH3:14])([CH3:13])[C:3]1[O:11][C:10]2[C:5](=[N+:6]([O-])[CH:7]=[CH:8][CH:9]=2)[CH:4]=1.O=P(Cl)(Cl)[Cl:17]>>[Cl:17][C:9]1[CH:8]=[CH:7][N:6]=[C:5]2[CH:4]=[C:3]([Si:2]([CH3:14])([CH3:13])[CH3:1])[O:11][C:10]=12
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 667793722-(Trimethylsilyl)furo[3,2-B]pyridine 4-oxide

생성물 1

HCID 594273397-Chloro-2-(trimethylsilyl)furo[3,2-b]pyridine

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온도
100 °C

실험 절차

2-(Trimethylsilyl)furo[3,2-b]pyridine N-oxide (10.51 g, 50.7 mmol) dissolved in POCl3 (47.3 ml, 507 mmol) in a sealed flask and heated at 100° C. for one hour. The reaction was cooled to RT, poured into a beaker washing with minimal DCM, and cooled in a brine bath. Saturated sodium bicarbonate solution was added very slowly and then solid sodium bicarbonate was added portion wise until the solution was at about pH=8. The solution was extracted twice with DCM, and the combined organic layers were dried with sodium sulfate, filtered, and concentrated. The material was purified via column chromatography (gradient elution 5-40% EtOAc:Hex) to afford 7-chloro-2-(trimethylsilyl)furo[3,2-b]pyridine as a pale yellow oil. MS: M+H+=226.2

후처리

  1. temperatureThe reaction was cooled to RT
  2. additionpoured into a beaker
  3. washwashing with minimal DCM
  4. temperaturecooled in a brine bath
  5. additionSaturated sodium bicarbonate solution was added very slowly
  6. additionsolid sodium bicarbonate was added portion wise until the solution
  7. extractionThe solution was extracted twice with DCM
  8. dry with materialthe combined organic layers were dried with sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe material was purified via column chromatography (gradient elution 5-40% EtOAc:Hex)

출처 및 근거

ORD 기록
ord-eabfc079b7824e7f8918f2d8c7d25fe0
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557816B2

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