Trifluoroacetic acid → Trifluoroacetate

HRID 1642058ノート

反応式

HRID 1642058 の反応式
[CH2:1]([O:3][C:4](=[O:24])[CH2:5][N:6]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1)[S:7]([NH:10]C(C)(C)C)(=[O:9])=[O:8])[CH3:2].[C:25]([OH:31])([C:27]([F:30])([F:29])[F:28])=[O:26]>O1CCOCC1>[CH2:1]([O:3][C:4](=[O:24])[CH2:5][N:6]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1)[S:7]([NH2:10])(=[O:9])=[O:8])[CH3:2].[F:28][C:27]([F:30])([F:29])[C:25]([O-:31])=[O:26]

参加物

5

反応物 2

HCID 6422Trifluoroacetic acidHCID 66755636HCID 66755636、化合物

生成物 2

HCID 84468TrifluoroacetateHCID 66755370(3-Nitro-phenyl-N-(aminosulfonyl)amino)-acetic acid ethyl ester

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

5 mmol of (3-nitro-phenyl-N-(t-butylaminosulfonyl)amino)-acetic acid ethyl ester is dissolved in 20 ml of 90% aqueous TFA and the mixture obtained is stirred for 1 hour at rt. The mixture obtained is diluted with dioxane and solvent is evaporated. (3-Nitro-phenyl-N-(aminosulfonyl)amino)-acetic acid ethyl ester in the form of a trifluoroacetate is obtained.

後処理

  1. customthe mixture obtained
  2. customThe mixture obtained
  3. customis evaporated

出典と根拠

ORDレコード
ord-33cc340f28a9432b8d1dfeb5c7afd54e
出典データセット
uspto-grants-2012_02
特許番号
US08119617B2

反応ノート

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