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Benzyl chloroformate → benzyl N-(4,4,4-trifluoro-1-hydroxybutan-2-yl)carbamate

HRID 1486256
ノート
印刷プレビュー

反応式

HRID 1486256 の反応式
[NH2:1][CH:2]([CH2:5][C:6]([F:9])([F:8])[F:7])[CH2:3][OH:4].C(=O)([O-])[O-].[K+].[K+].Cl[C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:18]>O1CCOCC1>[F:7][C:6]([F:9])([F:8])[CH2:5][CH:2]([NH:1][C:17](=[O:18])[O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:3][OH:4]
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 3

HCID 10387Benzyl chloroformate2 回HCID 11430Potassium Carbonate2 回HCID 534164332-Amino-4,4,4-trifluorobutan-1-ol

生成物 1

HCID 90136009benzyl N-(4,4,4-trifluoro-1-hydroxybutan-2-yl)carbamate

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

400 mg of rac-2-amino-4,4,4-trifluorobutan-1-ol (Example 42A, 2.5 mmol, purity about 90%, 1 equivalent) in 36 ml of 1,4-dioxane were admixed at RT with 0.38 ml of 50% aqueous potassium carbonate solution (1.7 mmol, 0.68 equivalent) and 0.54 ml of benzyl chloroformate (3.8 mmol, 1.5 equivalents), and the mixture was stirred at RT for 2 h. Then another 0.11 ml of benzyl chloroformate (0.76 mmol, 0.3 equivalent) and 0.08 ml of 50% aqueous potassium carbonate solution (0.35 mmol, 0.14 equivalent) were added and the mixture was stirred at RT for a further 30 min. Concentration under reduced pressure was followed by purification by means of preparative HPLC (RP18 column, eluent:acetonitrile/water gradient with addition of 0.1% TFA). The resulting crude product was taken up in ethyl acetate and washed twice with saturated aqueous sodium hydrogencarbonate solution. The aqueous phase was extracted with ethyl acetate, and the combined organic phases were dried over sodium sulphate, filtered and concentrated. 490 mg (70% of theory) of the title compound were obtained.

後処理

  1. stirringthe mixture was stirred at RT for a further 30 min
  2. concentrationConcentration under reduced pressure
  3. customwas followed by purification by means of preparative HPLC (RP18 column, eluent:acetonitrile/water gradient with addition of 0.1% TFA)
  4. washwashed twice with saturated aqueous sodium hydrogencarbonate solution
  5. extractionThe aqueous phase was extracted with ethyl acetate
  6. dry with materialthe combined organic phases were dried over sodium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-02c1ef926dab4bcea05c3fd960cb2d06
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09422285B2

反応ノート

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