Acetonitrile, difluoro- → Methyl 2-(difluoromethyl)-4,5-dihydrooxazole-4-carboxylate

HRID 1526604ノート

反応式

HRID 1526604 の反応式
C[O-].[Na+].[F:4][CH:5]([F:8])[C:6]#[N:7].Cl.[CH3:10][O:11][C:12](=[O:17])[CH:13]([CH2:15][OH:16])N>CO>[F:4][CH:5]([F:8])[C:6]1[O:16][CH2:15][CH:13]([C:12]([O:11][CH3:10])=[O:17])[N:7]=1

参加物

5

実験手順

To a cooled (0° C.) solution of sodium methoxide (25 wt % solution in methanol; 0.230 mL, 1.032 mmol) and MeOH (20 mL) was added dropwise difluoroacetonitrile (0.690 mL, 10.03 mmol) while maintaining an internal temperature of <1° C. After 20 min DL-serine methyl ester hydrochloride (1.55 g, 9.96 mmol) was added followed by MeOH (20 mL) and the reaction was allowed to warm to rt overnight. Subsequently, the reaction was heated to 55° C. for 5 h. The reaction was cooled to rt and partitioned between DCM/water. The aqueous layer was extracted with DCM (3×) and the combined organic layers were washed with water and dried over MgSO4. The filtrate was concentrated in vacuo to give 1.59 g (89%) of a light-brown oil. MS m/z=180 [M+H]+. Calculated for C6H7F2NO3:179.

後処理

  1. temperaturewhile maintaining an internal temperature of <1° C
  2. temperatureSubsequently, the reaction was heated to 55° C. for 5 h
  3. temperatureThe reaction was cooled to rt
  4. custompartitioned between DCM/water
  5. extractionThe aqueous layer was extracted with DCM (3×)
  6. washthe combined organic layers were washed with water
  7. dry with materialdried over MgSO4
  8. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-55f4bf2e098e4748920a2bc78e5442ee
出典データセット
uspto-grants-2015_07
特許番号
US09085576B2

反応ノート

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