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Diglyme → HCID 23455911、化合物

HRID 1680403
ノート
印刷プレビュー

反応式

HRID 1680403 の反応式
[F:1][C:2]([F:10])([F:9])[C:3]([C:5]([F:8])([F:7])[F:6])=[O:4].[F-:11].[K+].COCCOCCOC.Cl[C:23]([F:30])([F:29])[C:24]([Cl:28])=[C:25]([F:27])[F:26]>O>[F:11][C:3]([O:4][C:23]([F:30])([F:29])[C:24]([Cl:28])=[C:25]([F:27])[F:26])([C:5]([F:8])([F:7])[F:6])[C:2]([F:10])([F:9])[F:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8150Diglyme2 回HCID 12695HexafluoroacetoneHCID 522689Potassium FluorideHCID 125650472,3-Dichloro-1,1,3,3-tetrafluoroprop-1-ene

生成物 1

HCID 23455911HCID 23455911、化合物収率 39%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Hexafluoroacetone (16.6 g, 0.10 mol) was distilled into a stirred mixture of potassium fluoride (5.80 g, 0.10 mol) and 1-(2-methoxyethoxy)-2-methoxyethane (hereinafter referred to as diglyme) (100 ml) to give a homogeneous solution. This mixture was maintained at 25°-30° C. and treated with 1,2-dichloro-1,1,3,3-tetrafluoropropene (18.3 g, 0.10 mol, prepared according to J. E. Bissey, H. Goldwhite and D. G. Rowsell, J. Org. Chem., 32, 1542 (1967)). The mixture was stirred overnight and then it was poured into water (500 ml). The lower layer was washed with water (250 ml), dried, and distilled to give 1-(heptafluoro-2-propoxy)-1,1,3,3-tetrafluoro-2-chloropropene (13.0 g, 0.039 mol, 39%), bp 82°-83° C. whose structure was confirmed by the following: λmax 5.72 (CCl=CF2) and 7.5-10 μm (CF, C--O); 19F NMR, -64.9 (m) 2F, -- OCF2C=C; -76.0 (2nd order m) 2F, C=CF2 ; -81.2 (t J=5.7 Hz, each member d J=2.2 Hz) 6F, CF3 ; and -146.7 ppm (t J=22.9 Hz each member septet J=2.2 Hz) 1F, CFO.

後処理

  1. customto give a homogeneous solution
  2. temperatureThis mixture was maintained at 25°-30° C.
  3. washThe lower layer was washed with water (250 ml)
  4. customdried
  5. distillationdistilled

出典と根拠

ORDレコード
ord-8a9aec04a9214f1ea4bf555d20a319bb
出典データセット
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04273728

反応ノート

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