Trimethylpyruvic acid → HCID 54369426, 화합물

HRID 726869

반응식

HRID 726869 반응식
[CH3:1][C:2]([CH3:14])([CH3:13])[CH:3]=[N:4][C@H:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH3:6].CC(C)(C)C(=O)[C:18]([OH:20])=[O:19]>C(OCC)C>[CH3:14][C:2]([CH3:13])([CH3:1])[C:3](=[N:4][C@H:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH3:6])[C:18]([OH:20])=[O:19]

참가 물질

4

반응물 2

HCID 13150Trimethylpyruvic acidHCID 10921316HCID 10921316, 화합물

생성물 1

HCID 54369426HCID 54369426, 화합물수율 81.2%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

반응 조건

온도
0 °C

실험 절차

8.9 g (47 mmol) of (S)-(2,2-dimethylpropylidene)-(1-phenylethyl)-amine (J. L. Fauchure, C. Petermann, Helv. Chim. Acta 1980, 63, 824) were dissolved in 10 ml of diethyl ether with the exclusion of moisture. 8.1 g (50 mmol) of trimethylpyruvic acid in 10 ml of diethyl ether were added dropwise to this solution while cooling with ice. Subsequently, the mixture was stirred at 0° C. for a further 2 hours and at room temperature for 6 hours. Colorless crystals form over 2 days and these were suspended in 50 ml of diethyl ether, filtered off and washed twice with 5 ml of diethyl ether each time. After drying in a vacuum there were obtained 8.9 g (81%) of (S)-3,3-dimethyl-2-(1-phenylethylimino)-butyric acid (internal salt) of melting point 135°-136° C. [α]=-14.4 (c=0.16, CH2Cl2).

후처리

  1. temperaturewhile cooling with ice
  2. customColorless crystals form over 2 days
  3. filtrationfiltered off
  4. washwashed twice with 5 ml of diethyl ether each time
  5. customAfter drying in a vacuum there

출처 및 근거

ORD 기록
ord-c251794771034e39bfe469d983ba6813
출처 데이터셋
uspto-grants-1998_01
특허 번호
US05710322

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