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Trifluoroacetic acid → HCID 68533409、化合物

HRID 401810
ノート
印刷プレビュー

反応式

HRID 401810 の反応式
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH2:10][C:11]2=[O:16])(C)(C)C.[C:18]([OH:24])([C:20]([F:23])([F:22])[F:21])=[O:19]>C(Cl)Cl>[F:21][C:20]([F:23])([F:22])[C:18]([OH:24])=[O:19].[NH2:7][CH:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH2:10][C:11]2=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 68535128HCID 68535128、化合物

生成物 1

HCID 68533409HCID 68533409、化合物収率 92%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

(5-Oxo-bicyclo[2.2.2]oct-2-yl)-carbamic acid tert-butyl ester (Preparation 75, 279 g, 1.17 mol, 1.0 eq) was taken up in DCM (450 mL). TFA (416 mL, 5.60 mol, 4.8 eq) was added dropwise. On addition, the reaction warms to reflux while much gas evolves. The reaction mixture was kept at reflux temperature for 1 hour after which it was allowed to cool to room temperature overnight. The mixture was concentrated and the residue was taken up in DCM (50 mL) and then tert-butyl methyl ether (1.3 L) was added which resulted in a brown suspension. The solids were collected by filtration (P3) and were washed with tert-butyl methyl ether. The latter was dried in vacuo (40° C.) to furnish title compound as an off-white solid (272 g, 1.07 mol, 92%).

後処理

  1. additionOn addition
  2. temperatureto reflux while much gas evolves
  3. temperatureat reflux temperature for 1 hour after which it
  4. concentrationThe mixture was concentrated
  5. additiontert-butyl methyl ether (1.3 L) was added which
  6. customresulted in a brown suspension
  7. filtrationThe solids were collected by filtration (P3)
  8. washwere washed with tert-butyl methyl ether
  9. customThe latter was dried in vacuo (40° C.)

出典と根拠

ORDレコード
ord-e45bafd565604a84b9b5ed03ef2f7976
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08741934B2

反応ノート

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