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Gamma-Aminobutyric Acid → Glutamic acid, 5-(1,1-dimethylethyl) ester

HRID 732865
ノート
印刷プレビュー

反応式

HRID 732865 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][C:5]([OH:7])=[O:6].[OH-].[Na+].C([O:14][C:15](OC(OC(C)(C)C)=O)=[O:16])(C)(C)C.O.[C:26](O)([CH3:29])([CH3:28])[CH3:27]>>[C:5]([CH2:4][CH2:3][CH:2]([NH2:1])[C:15]([OH:16])=[O:14])([O:7][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:6]
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 5

HCID 119Gamma-Aminobutyric AcidHCID 962WaterHCID 6386tert-Butanol2 回HCID 14798Sodium HydroxideHCID 90495Di-tert-butyl dicarbonate

生成物 1

HCID 3431852Glutamic acid, 5-(1,1-dimethylethyl) ester

実験手順

4-Aminobutanoic acid (1 g, 9.7 mmol) was dissolved in tert-butyl alcohol (15 ml), 5N NaOH (1.93 ml, 9.7 mmol) was added thereto, and the mixture was stirred at room temperature for 10 minutes. Di-tert-butyl-dicarbonate (2.33 g, 10.7 mmol) dissolved in tert-butylalcohol (17 ml) was added thereto and stirred for 24 hours at room temperature. Water (12 ml) was added thereto and the resultant was concentrated under a reduced pressure and cooled to 0° C. Then, 2N H2SO4 was added thereto dropwise until pH of the mixture became 2. The resultant was extracted with ethyl acetate and the extract was washed with water. The organic layer was dried over MgSO4 and concentrated to obtain the title compound (2.1 g) as a white solid.

後処理

  1. additionwas added
  2. stirringstirred for 24 hours at room temperature
  3. concentrationthe resultant was concentrated under a reduced pressure
  4. temperaturecooled to 0° C
  5. additionThen, 2N H2SO4 was added
  6. extractionThe resultant was extracted with ethyl acetate
  7. washthe extract was washed with water
  8. dry with materialThe organic layer was dried over MgSO4
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-0eaaf035a053449f9a730905a7037da5
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07589072B2

反応ノート

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