Water → HCID 178500188、化合物

HRID 40429

反応式

HRID 40429 の反応式
[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8])#[N:2].[Cl-].C([NH+](CC)CC)C.[N-:19]=[N+:20]=[N-:21].[Na+].O>C1(C)C=CC=CC=1>[NH:2]1[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8])=[N:21][N:20]=[N:19]1

参加物

6

反応物 4

HCID 962WaterHCID 33557Sodium AzideHCID 554130Methyl 5-cyanopentanoateHCID 12698378Triethylazanium chloride

生成物 1

HCID 178500188HCID 178500188、化合物収率 68%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

Methyl 5-cyanopentanoate (4.8 g, 34 mmol) is dissolved in toluene, triethylammonium chloride (14 g, 102 mmol) and sodium azide (6.63, 102 mmol) is added. The mixture is heated to reflux for overnight. The reaction mixture is cooled to room temperature, water is added to extract (3×100 mL) methyl 5-tetrazol-5-ylpentanoate from the organic. To the aqueous phase, concentrate HCl is added to adjust pH to 2. The product is extracted from the aqueous solution with EtOAc (3×50 mL). The organic is combined, dried and concentrated to yield 4.25 g (68%) of methyl 5-tetrazol-5-ylpentanoate.

後処理

  1. temperatureThe mixture is heated
  2. temperatureto reflux for overnight
  3. extractionto extract (3×100 mL) methyl 5-tetrazol-5-ylpentanoate from the organic
  4. concentrationTo the aqueous phase, concentrate HCl
  5. additionis added
  6. extractionThe product is extracted from the aqueous solution with EtOAc (3×50 mL)
  7. customdried
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7cde7874cf74436290aebec88000a3ab
出典データセット
uspto-grants-2013_09
特許番号
US08529882B2

関連ノート

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