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Sodium Nitrite → HCID 58136805, 화합물

HRID 657988
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HRID 657988 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 (O4.050; 3.00 g) was dissolved in 35% aqueous sulfuric acid (25 ml) while heating. 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. temperaturewhile heating
  2. customthe cooling bath was removed
  3. temperaturethe mixture was heated to 100° C. for 2 h
  4. temperatureAfter cooling
  5. extractionthe mixture was extracted twice with EA
  6. washThe combined EA phases were washed with saturated sodium hydrogencarbonate solution
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residue was purified
  11. customsilica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-100% within 40 min)

출처 및 근거

ORD 기록
ord-a8345a17ba2740dabb86fb940532d074
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08076336B2

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