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Sodium Nitrite → HCID 58136805、化合物

HRID 657988
ノート
印刷プレビュー

反応式

HRID 657988 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

HCID 58136805HCID 58136805、化合物収率 54.7%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 1118Sulfuric Acid溶媒

反応条件

温度
-5 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-a8345a17ba2740dabb86fb940532d074
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08076336B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート