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Isobutyraldehyde → (4S)-4-Isobutyl-2-isopropyloxazolidine

HRID 276259
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HRID 276259 반응식
[OH:1][CH2:2][C@@H:3]([NH2:8])[CH2:4][CH:5]([CH3:7])[CH3:6].[CH:9](=O)[CH:10]([CH3:12])[CH3:11]>C1(C)C=CC=CC=1>[CH:10]([CH:12]1[NH:8][C@@H:3]([CH2:4][CH:5]([CH3:7])[CH3:6])[CH2:2][O:1]1)([CH3:11])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6561IsobutyraldehydeHCID 111307L-Leucinol

생성물 1

HCID 45096513(4S)-4-Isobutyl-2-isopropyloxazolidine수율 100.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of (1S)-1-(hydroxymethyl)-3-methylbutylamine (Method B1b; 152 g, 1.3 mol) and isobutyraldehyde (118 mL, 1.3 mol, 1.0 equiv.) in toluene (1.5 L) was heated at the reflux temp. until the theoretical amount of water had been collected in a Dean-Stark trap (23.4 mL). The reaction mixture was concentrated by distillation to approximately 700 mL. The resulting mixture was cooled to room temp. and was concentrated under reduced pressure to a constant weight to give (4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine as a pale yellow oil (223 g, 100%): 1H NMR (CDCl3) δ0.88-0.99 (m, 12H), 1.18-1.35 (m, 1H), 1.42-1.56 (m, 1H), 1.61-1.79 (m, 4H), 3.08 (t, J=7.4 Hz 1H), 3.20-3.34 (m, 1H), 3.85 (t, J=7.4 Hz, 1H), 4.18 (dd, J=7.3, 3.4 Hz, 1H).

후처리

  1. customuntil the theoretical amount of water had been collected in a Dean-Stark trap (23.4 mL)
  2. concentrationThe reaction mixture was concentrated by distillation to approximately 700 mL
  3. temperatureThe resulting mixture was cooled to room temp.
  4. concentrationwas concentrated under reduced pressure to a constant weight

출처 및 근거

ORD 기록
ord-71ca128157574f968e5f7a17729a53c5
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06353006B1

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