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Water → (2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-ol

HRID 731018
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HRID 731018 반응식
Cl[CH2:2][C@:3]([C:8]1[CH:13]=[CH:12][C:11]([F:14])=[CH:10][C:9]=1[F:15])([OH:7])[C@H:4]([OH:6])[CH3:5].C[O-].[Na+].O>CO>[O:7]1[C@:3]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][C:9]=2[F:15])([C@H:4]([OH:6])[CH3:5])[CH2:2]1
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5

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HCID 962WaterHCID 10942334Sodium MethoxideHCID 67175587(2R,3R)-1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diol

생성물 1

HCID 10867332(2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-ol수율 97%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of 1.00 g (4.23 mmol) of (2R,3R)-1-chloro-2-(2,4-difluorophenyl)butane-2,3-diol in 8 mL of methanol was cooled in ice, and 0.91 g (4.65 mmol) of a 28% solution of NaOMe in methanol was added thereto. The reaction was performed for 2 hours, and 10 mL of water was added to stop the reaction. Then, extraction was performed with 20 mL of ethyl acetate. After drying over anhydrous sodium sulfate, concentration was performed under reduced pressure to obtain a crude product. The product was quantitatively analyzed by HPLC (under the same HPLC measurement conditions as those in Example 10). The title compound was obtained in a yield of 97%. 1H-NMR (400 MHz, CDCl3) δ: 1.19 (d, 3H, J=6.3 Hz), 2.22 (s, 1H), 2.91 (d, 1H, J=4.9 Hz), 3.28 (d, 1H, J=4.9 Hz), 4.11 (d, 1H, J=6.3 Hz), 6.80-6.91 (m, 2H), 7.34-7.39 (m, 1H).

후처리

  1. customthe reaction
  2. extractionThen, extraction
  3. dry with materialAfter drying over anhydrous sodium sulfate, concentration
  4. customto obtain a crude product

출처 및 근거

ORD 기록
ord-271b56d281184035ade6144bb96207f2
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582781B2

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