Methyl 2-chloroacrylate → HCID 11034029、化合物

HRID 849275ノート

反応式

HRID 849275 の反応式
[F:1][C:2]([F:15])([F:14])[CH2:3][N:4]=[C:5](Cl)[C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[CH:8][CH:7]=1.Cl[C:17](=[CH2:22])[C:18]([O:20][CH3:21])=[O:19].N12CCCN=C1CCCCC2>CN(C)C=O>[Cl:12][C:9]1[CH:10]=[CH:11][C:6]([C:5]2[NH:4][C:3]([C:2]([F:15])([F:14])[F:1])=[CH:22][C:17]=2[C:18]([O:20][CH3:21])=[O:19])=[CH:7][CH:8]=1

参加物

5

反応物 3

HCID 6659Methyl 2-chloroacrylateHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 11807271Benzenecarboximidoyl chloride, 4-chloro-N-(2,2,2-trifluoroethyl)-

生成物 1

HCID 11034029HCID 11034029、化合物収率 34.6%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of N-(2,2,2-trifluoroethyl)-4-chlorobenzimidoyl chloride (10.2 g, 0.04 mol) and methyl 2-chloroacrylate (5.8 g, 0.048 mol) in N,N-dimethylformamide is treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 19.5 g, 0.128 mol) over 30 minutes at such a rate that the temperature is kept at 40° C., stirred for two hours, and quenched with water and ethyl acetate. The organic layer is separated, washed sequentially with aqueous HCl and water, and concentrated in vacuo to obtain an oil. Flash column chromatography of the oil using silica gel and a 20% ethyl acetate in heptane solution and crystallization from heptane gives the title product as white crystals (4.2 g, 34.6% yield, mp 120.0-122.5° C.)

後処理

  1. customis kept at 40° C.
  2. customquenched with water and ethyl acetate
  3. customThe organic layer is separated
  4. washwashed sequentially with aqueous HCl and water
  5. concentrationconcentrated in vacuo
  6. customto obtain an oil
  7. customa 20% ethyl acetate in heptane solution and crystallization from heptane

出典と根拠

ORDレコード
ord-1b29870133c948a0bbe0386f4ccf5867
出典データセット
uspto-grants-2000_01
特許番号
US06011161

反応ノート

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