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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Propanol, 2,2,3,3,3-pentafluoro-1-methoxy- → (4S)-4-isobutyl-2-(pentafluoroethyl)-1,3-oxazolidine

HRID 1009249
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HRID 1009249 반응식
[CH3:1][O:2][CH:3](O)[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6].[NH2:12][C@H:13](CO)[CH2:14][CH:15]([CH3:17])[CH3:16]>C1C=CC=CC=1>[CH2:14]([C@H:13]1[CH2:1][O:2][CH:3]([C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6])[NH:12]1)[CH:15]([CH3:17])[CH3:16]
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참가 물질

4

반응물 2

HCID 1084041-Propanol, 2,2,3,3,3-pentafluoro-1-methoxy-HCID 111307L-Leucinol

생성물 1

HCID 11413942(4S)-4-isobutyl-2-(pentafluoroethyl)-1,3-oxazolidine

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

Pentafluoropropanal methyl hemiacetal (14.9 g, 82.8 mmol) and L-leucinol (9.7 g, 82.8 mmol) were dissolved in 100 mL of benzene and heated to reflux overnight in a flask equipped with a Dean-Stark tube. The resulting solution was cooled and concentrated to provide the title compound as an oil which was used directly in the following step.

후처리

  1. temperatureheated
  2. temperatureto reflux overnight in a flask
  3. customequipped with a Dean-Stark tube
  4. temperatureThe resulting solution was cooled
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-cc13fbe8013b439d9b49cec9ee72cfec
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973037B2

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