Diethyl Ether → Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetate

HRID 128590

反応式

HRID 128590 の反応式
[CH3:1][CH2:2][O:3][CH2:4]C.[OH-].[K+].N(CNC(N)=O)=[O:9].[CH3:15][O:16][C:17]1[CH:25]=[C:24]([O:26][CH:27]2[CH2:32][CH2:31][N:30]([C:33]([O:35][C:36]([CH3:39])([CH3:38])[CH3:37])=[O:34])[CH2:29][CH2:28]2)[CH:23]=[CH:22][C:18]=1C(Cl)=O>C1COCC1>[CH3:15][O:16][C:17]1[CH:25]=[C:24]([O:26][CH:27]2[CH2:28][CH2:29][N:30]([C:33]([O:35][C:36]([CH3:37])([CH3:39])[CH3:38])=[O:34])[CH2:31][CH2:32]2)[CH:23]=[CH:22][C:18]=1[CH2:1][C:2]([O:3][CH3:4])=[O:9]

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 14797Potassium HydroxideHCID 104823Urea, (nitrosomethyl)-HCID 189141552-methoxy-4-(1-Boc-4-piperidyloxy)benzoyl chloride

生成物 1

HCID 18914175Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of ether (66 ml) and 40% aqueous potassium hydroxide (20 ml) was cooled in ice. N-Nitrosomethylurea (6.6 g) was added in portions with gentle swirling over 30 min. The ether layer was decanted and dried over solid potassium hydroxide for 15 min. The ether solution was decanted, and the decanted solution was cooled in an ice bath. A solution of 2-methoxy-4-(1-Boc-4-piperidyloxy)benzoyl chloride (3.26 g, 8.8 mmol) in THF (6 ml) was added dropwise and the mixture was stirred in the cold for 15 min and at ambient temperature for 3.5 hours. Nitrogen was passed through the mixture for 1 hour, and the solution was then concentrated in vacuo. A portion (930 mg) of the residue was dissolved in methanol and heated to reflux, and a solution of silver benzoate (200 mg) in triethylamine (2 ml) was added in five 0.1 ml portions at intervals of eight minutes. A sixth portion was added after an additional forty minutes' reflux, and after another five minutes, a seventh portion. After a final 30 minutes' reflux, the mixture was cooled and filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel eluted with 3%, followed by 5% methanol in methylene chloride. The product fractions were combined and evaporated to dryness in vacuo to give methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)-phenylacetate.

後処理

  1. temperaturewas cooled in ice
  2. customThe ether layer was decanted
  3. dry with materialdried over solid potassium hydroxide for 15 min
  4. customThe ether solution was decanted
  5. temperaturethe decanted solution was cooled in an ice bath
  6. waitat ambient temperature for 3.5 hours
  7. waitNitrogen was passed through the mixture for 1 hour
  8. concentrationthe solution was then concentrated in vacuo
  9. dissolutionA portion (930 mg) of the residue was dissolved in methanol
  10. temperatureheated
  11. temperatureto reflux
  12. additiona solution of silver benzoate (200 mg) in triethylamine (2 ml) was added in five 0.1 ml portions at intervals of eight minutes
  13. additionA sixth portion was added after an additional forty minutes'
  14. temperaturereflux
  15. waitafter another five minutes
  16. temperatureAfter a final 30 minutes' reflux
  17. temperaturethe mixture was cooled
  18. filtrationfiltered
  19. concentrationthe filtrate was concentrated in vacuo
  20. customThe residue was chromatographed on silica gel
  21. washeluted with 3%
  22. customevaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-1759206d62554e9db68d9407fb9fe857
出典データセット
uspto-grants-1995_11
特許番号
US05464788

関連ノート

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