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Ethyl 4,4,4-trifluoroacetoacetate → CID 90109439

HRID 1508936
ノート
印刷プレビュー

反応式

HRID 1508936 の反応式
[CH:1]1([C:6](=[NH:8])[NH2:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[F:9][C:10]([F:20])([F:19])[C:11](=O)[CH2:12][C:13](OCC)=[O:14].C[O-].[Na+]>C(O)C>[CH:1]1([C:6]2[N:7]=[C:13]([OH:14])[CH:12]=[C:11]([C:10]([F:20])([F:19])[F:9])[N:8]=2)[CH2:5][CH2:4][CH2:3][CH2:2]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 3

HCID 67793Ethyl 4,4,4-trifluoroacetoacetateHCID 4452694CyclopentanecarboximidamideHCID 10942334Sodium Methoxide

生成物 1

HCID 178516140CID 90109439収率 36%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
85 °C

実験手順

To a solution of cyclopentanecarboximidamide (3.0 g, 27.1 mmol) in ethanol (100 mL) was added ethyl 4,4,4-trifluoro-3-oxobutanoate (5.0 g, 27.1 mmol) and sodium methoxide (1.76 g, 32.5 mmol). The mixture was stirred at 85° C. for 16 h. After this time, the mixture was concentrated, diluted with ethanol (10 mL), and the suspension was chilled to 0° C. HCl (2M, 50 mL) was added and the suspension was filtered and washed with water. The solid was dried under heat and vacuum to afford the title compound (2.24 g, 36%) as a white solid. MW=232.20. 1H NMR (DMSO-d6, 500 MHz) δ 12.96 (s, 1H), 6.67 (s, 1H), 3.03 (quin, J=8.2 Hz, 1H), 2.00-1.92 (m, 2H), 1.83-1.67 (m, 4H), 1.64-1.53 (m, 2H); APCI MS m/z 233 [M+H]+.

後処理

  1. concentrationAfter this time, the mixture was concentrated
  2. additiondiluted with ethanol (10 mL)
  3. temperaturethe suspension was chilled to 0° C
  4. additionHCl (2M, 50 mL) was added
  5. filtrationthe suspension was filtered
  6. washwashed with water
  7. customThe solid was dried
  8. temperatureunder heat

出典と根拠

ORDレコード
ord-7c18efbbe44b4843a10f55b107f3c576
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221843B2

反応ノート

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