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Water → tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate

HRID 896923
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HRID 896923 반응식
[H-].C([Al+]CC(C)C)C(C)C.CC[O:13][C:14]([C@@H:16]1[CH2:20][CH2:19][CH2:18][N:17]1[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])=O.O>C1(C)C=CC=CC=1.C(OCC)C>[C:24]([O:23][C:21]([N:17]1[CH2:18][CH2:19][CH2:20][C@H:16]1[CH:14]=[O:13])=[O:22])([CH3:27])([CH3:25])[CH3:26]
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참가 물질

6

반응물 3

HCID 962WaterHCID 10857688(S)-1-tert-butyl 2-ethyl pyrrolidine-1,2-dicarboxylateHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 2734674tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate수율 71.2%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 3283
Diethyl Ether
용매

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온도
-78 °C

실험 절차

At −78° C., a 1.2 M solution of diisobutylaluminum hydride (31.7 ml, 38 mmol) in toluene was added dropwise to a solution of (2S)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (4.02 g, 16.5 mmol) in diethyl ether (1.5 ml). The reaction mixture was stirred for 3 h at −78° C. Water (9.9 ml) was added dropwise. The reaction mixture was warmed to room temperature. The mixture was filtered through a plug of celite. The celite was washed with tert-butyl methyl ether (3×100 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo, to give 2.34 g of crude N-t-butyloxycarbonyl-(S)-prolinal, which was used for the next step without further purification.

후처리

  1. temperatureThe reaction mixture was warmed to room temperature
  2. filtrationThe mixture was filtered through a plug of celite
  3. washThe celite was washed with tert-butyl methyl ether (3×100 ml)
  4. dry with materialThe combined organic layers were dried over magnesium sulfate
  5. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-6a4543f47ca04c0c81c04623c40bb4f1
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06919315B1

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