Methyl Myristate → HCID 19780334、化合物

HRID 2081664

反応式

HRID 2081664 の反応式
[Na].[C:2]([NH:5][OH:6])([NH2:4])=[NH:3].OS(O)(=O)=O.CO[C:14](=O)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27]>C(O)C>[NH2:3][C:2]1[N:4]=[C:27]([CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH3:14])[O:6][N:5]=1

参加物

5

反応物 3

HCID 31284Methyl MyristateHCID 5360545SodiumHCID 178513206HCID 178513206、化合物

生成物 1

HCID 19780334HCID 19780334、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Sodium metal (1.6 g, 0.068 mol) was added to 4 Å molecular sieves (12 g) and ethanol (200 mL) under nitrogen. The mixture was stirred for 15 minutes, then hydroxyguanidine sulfate (9.32 g, 0.035 mol) added and the mixture stirred for 30 minutes. Methyltetradecanoate (1.43 g, 0.006 mol) was then added and the mixture refluxed for 1.5 hours, allowed to cool, filtered, and concentrated. The concentrate was partitioned between CH2Cl2 and water. The organic layer was washed with water and brine, dried with Na2SO4, filtered, concentrated, and triturated with hexane. The resulting solid was filtered, washed with hexane, and dried in vacuo to yield 0.23 g, m.p. 90°-91° C.

後処理

  1. stirringthe mixture stirred for 30 minutes
  2. temperaturethe mixture refluxed for 1.5 hours
  3. temperatureto cool
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe concentrate was partitioned between CH2Cl2 and water
  7. washThe organic layer was washed with water and brine
  8. dry with materialdried with Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customtriturated with hexane
  12. filtrationThe resulting solid was filtered
  13. washwashed with hexane
  14. customdried in vacuo
  15. customto yield 0.23 g, m.p. 90°-91° C.

出典と根拠

ORDレコード
ord-629bdb03c25041b29434fa130bb592ee
出典データセット
uspto-grants-1993_02
特許番号
US05185358

関連ノート

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