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Thiophosgene → HCID 86720971、化合物

HRID 524916
ノート
印刷プレビュー

反応式

HRID 524916 の反応式
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[NH2:8].[C:9](Cl)(Cl)=[S:10]>C1(C)C=CC=CC=1.CO.C(Cl)Cl>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[N:8]=[C:9]=[S:10]
参加物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 10040ThiophosgeneHCID 260954-Amino-3-bromopyridine

生成物 1

HCID 86720971HCID 86720971、化合物収率 57%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒2 回HCID 21226129Dichloromethane methanol溶媒

実験手順

3-bromopyridin-4-amine (5 g, 28.90 mmol) was suspended in dry toluene (100 mL) and cooled in an ice-bath. A solution of thiophosgene (6.646 g, 4.407 mL, 57.80 mmol) in dry toluene (100 mL) was added dropwise over 25 mins. The resulting orange/red suspension was stirred at reflux overnight. The red suspension was allowed to cool to RT and concentrated under reduced pressure to give a dark brown/red solid. This material was partitioned between saturated NaHCO3 and DCM. The aqueous layer was extracted with further DCM (3×50 mL) and the combined organics were dried over Na2SO4, filtered and concentrated under reduced pressure to give a dark red solid/gum. This material was suspended in MeOH/DCM, adsorbed onto silica under reduced pressure and purified by column chromatography (75% EtOAc in hexanes, ˜300 mL silica) to give 3-bromo-4-isothiocyanatopyridine as a red oil which solidified on standing (3.513 g, 57% Yield). MS (ES+) 216.9.

後処理

  1. temperaturecooled in an ice-bath
  2. temperatureat reflux overnight
  3. concentrationconcentrated under reduced pressure
  4. customto give a dark brown/red solid
  5. customThis material was partitioned between saturated NaHCO3 and DCM
  6. extractionThe aqueous layer was extracted with further DCM (3×50 mL)
  7. dry with materialthe combined organics were dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customto give a dark red solid/gum
  11. custompurified by column chromatography (75% EtOAc in hexanes, ˜300 mL silica)

出典と根拠

ORDレコード
ord-a558ebd93d7948828505b33a6e369352
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09340546B2

反応ノート

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