Phenol → 2-(2-Allyloxy4-nitrophenoxymethyl)-oxirane

HRID 28458

反応式

HRID 28458 の反応式
[H-].[Na+].[CH2:3]([O:6][C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[CH:9][C:8]=1[OH:16])[CH:4]=[CH2:5].[C:17]1([OH:23])C=CC=[CH:19][CH:18]=1.S(C1C=CC(C)=CC=1)(OC[C@@H]1OC1)(=O)=O>>[CH2:3]([O:6][C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[CH:9][C:8]=1[O:16][CH2:19][CH:18]1[CH2:17][O:23]1)[CH:4]=[CH2:5]

参加物

5

反応物 4

HCID 996PhenolHCID 24758Sodium hydrideHCID 154187Glycidyl tosylate, (R)-HCID 120822032-Allyloxy-4-nitrophenol

生成物 1

HCID 218920512-(2-Allyloxy4-nitrophenoxymethyl)-oxirane

実験手順

20 g (0.50 mole) of 60% NaH/mineral oil was placed in a two-liter flask and washed with 500 mL of hexane. 1 L of DMF was added, followed by 77 g (0.40 mole) of the 2-allyloxy-4-nitrophenol prepared in the previous step. Addition of the phenol was performed in portions under argon. After stirring the mixture for 30 minutes at room temperature under argon, 108 g (0.48 moles) of (R)-glycidyl tosylate was added and the mixture heated at 70-75° C. under nitrogen overnight. Upon cooling, the DMF was removed in vacuum and replaced with one liter of methylene chloride. This was washed with 500 mL portions of 2 N HCl, saturated sodium bicarbonate and saturated brine and dried over sodium sulfate. The mixture was filtered, concentrated to an oil in vacuum and column chromatographed on silica gel using 1:1 hexane/methylene chloride as eluent. This gave 43 g of product contaminated with traces of the two starting materials, followed by 21 g of pure product as a pale yellow solid. The impure material was recrystallized from 1.2 L of 10% ethyl acetate/hexane to give 34 g of pure (homogeneous on silica gel tlc with 1:1 hexane/methylene chloride) (R)-2-(2-allyloxy-4-nitrophenoxymethyl)-oxirane (m.p. 64° C.).

後処理

  1. washwashed with 500 mL of hexane
  2. addition1 L of DMF was added
  3. customprepared in the previous step
  4. temperaturethe mixture heated at 70-75° C. under nitrogen overnight
  5. temperatureUpon cooling
  6. customthe DMF was removed in vacuum
  7. washThis was washed with 500 mL portions of 2 N HCl, saturated sodium bicarbonate and saturated brine
  8. dry with materialdried over sodium sulfate
  9. filtrationThe mixture was filtered
  10. concentrationconcentrated to an oil in vacuum and column
  11. customchromatographed on silica gel using 1:1 hexane/methylene chloride as eluent
  12. customThe impure material was recrystallized from 1.2 L of 10% ethyl acetate/hexane
  13. customto give 34 g of pure (homogeneous on silica gel tlc with 1:1 hexane/methylene chloride) (R)-2-(2-allyloxy-4-nitrophenoxymethyl)-oxirane (m.p. 64° C.)

出典と根拠

ORDレコード
ord-381e385a3ea246718b7ab20b7be83cb3
出典データセット
uspto-grants-2008_09
特許番号
US07419986B2

関連ノート

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