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Sodium Nitrite → HCID 58136805, 화합물

HRID 1258532
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HRID 1258532 반응식
N[C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1.N([O-])=[O:18].[Na+]>S(=O)(=O)(O)O.O>[OH:18][C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1
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참가 물질

5

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HCID 23668193Sodium NitriteHCID 581368521-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone

생성물 1

HCID 58136805HCID 58136805, 화합물수율 54.7%

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매

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온도
-5 °C

실험 절차

1-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone (3.00 g) was dissolved while heating in 35% aqueous sulfuric acid (25 ml). The solution was cooled to −5° C. and a solution of sodium nitrite (780 mg) in 15 ml of water was added dropwise within 10 min. After 40 min at −5° C., the cooling bath was removed and the mixture was heated to 100° C. for 2 h. After cooling, the mixture was extracted twice with EA. The combined EA phases were washed with saturated sodium hydrogencarbonate solution, dried, filtered and concentrated. The residue was purified using silica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-100% within 40 min). 1.62 g of the title compound were obtained.

후처리

  1. customthe cooling bath was removed
  2. temperaturethe mixture was heated to 100° C. for 2 h
  3. temperatureAfter cooling
  4. extractionthe mixture was extracted twice with EA
  5. washThe combined EA phases were washed with saturated sodium hydrogencarbonate solution
  6. customdried
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified
  10. customsilica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-100% within 40 min)

출처 및 근거

ORD 기록
ord-720e663eaed64bcf8ac71861e0931030
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08466169B2

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