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Hydrochloric Acid → 5-(3-Methoxyphenyl)-4-nitrovaleric acid

HRID 274071
ノート
印刷プレビュー

反応式

HRID 274071 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH:10]([N+:20]([O-:22])=[O:21])[CH2:11][CH2:12][C:13]([O:15]C(C)(C)C)=[O:14])[CH:6]=[CH:7][CH:8]=1.Cl.[Cl-].[Na+].C(=O)([O-])O.[Na+]>O1CCOCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH:10]([N+:20]([O-:22])=[O:21])[CH2:11][CH2:12][C:13]([OH:15])=[O:14])[CH:6]=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 516892Sodium BicarbonateHCID 20094814Tert-butyl 5-(3-methoxyphenyl)-4-nitrovalerate

生成物 1

HCID 200948615-(3-Methoxyphenyl)-4-nitrovaleric acid収率 97.7%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane
溶媒
2 回

実験手順

To a solution of tert-butyl 5-(3-methoxyphenyl)-4-nitrovalerate (10.00 g) in 1,4-dioxane (10 ml) was added 4N hydrogen chloride in 1,4-dioxane (17.8 ml) in an ice bath. After stirring for 3 days at ambient temperature, ice water (60 ml) and sodium chloride (6 g) was added to the solution. The pH of the solution was adjusted to 9.5 with an aqueous saturated sodium hydrogencarbonate solution and the solution was washed with ethyl acetate. After the pH of the solution was adjusted to 1 with 6N hydrochloric acid, the solution was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous sodium sulfate, treated with silica gel (20 g), and evaporated in vacuo to give 5-(3-methoxyphenyl)-4-nitrovaleric acid (8.00 g).

後処理

  1. washthe solution was washed with ethyl acetate
  2. extractionthe solution was extracted with ethyl acetate
  3. washThe extract was washed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. additiontreated with silica gel (20 g)
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-8d8aa8ff40364c3790df6f32bd84df76
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05387710

反応ノート

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