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Formamide → HCID 178461168、化合物

HRID 335135
ノート
印刷プレビュー

反応式

HRID 335135 の反応式
[NH2:1][C:2]1[CH2:6][CH2:5][C@@H:4]([CH3:7])[C:3]=1[C:8]([O:10]CC)=O.C([O-])=O.[NH4+].[CH:17]([NH2:19])=O>C1(C)C=CC=CC=1>[CH3:7][C@H:4]1[C:3]2[C:8]([OH:10])=[N:19][CH:17]=[N:1][C:2]=2[CH2:6][CH2:5]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 713FormamideHCID 2723923Ammonium formateHCID 59671147Ethyl (5R)-2-amino-5-methyl-1-cyclopentene-1-carboxylate

生成物 1

HCID 178461168HCID 178461168、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
150 °C

実験手順

A 2 L 3-neck round bottom flask equipped with a condenser, internal temperature probe, was charged with (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (185 g, 1093 mmol) and ammonium formate (103.4 g, 1640 mmol) in formamide (400 mL) and toluene (200 mL). The reaction was heated to an internal temperature of 150° C. and stirred for 36 hours. The reaction was cooled and transferred to a 2 L single next flask and excess formamide was removed by high vacuum distillation. The resulting oil was dissolved in CH2Cl2 and washed with brine. The combined aqueous layers were extracted with CH2Cl2. The combined organic layers were dried over sodium sulfate, filtered and concentrated to give the crude product as a brown semi solid which was taken into the next step without any further purification.

後処理

  1. customA 2 L 3-neck round bottom flask equipped with a condenser
  2. temperatureThe reaction was cooled
  3. customtransferred to a 2 L single next flask
  4. customexcess formamide was removed by high vacuum distillation
  5. dissolutionThe resulting oil was dissolved in CH2Cl2
  6. washwashed with brine
  7. extractionThe combined aqueous layers were extracted with CH2Cl2
  8. dry with materialThe combined organic layers were dried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-25030f1a459642fca995b2b0371e37c0
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08883828B2

反応ノート

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