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Carbon Dioxide → 3-(Chloromethoxy)-1,1,1,2,2-pentafluoropropane

HRID 267649
ノート
印刷プレビュー

反応式

HRID 267649 の反応式
[F:1][C:2]([F:10])([C:6]([F:9])([F:8])[F:7])[CH2:3][O:4][CH3:5].C(=O)=O.S(Cl)([Cl:17])(=O)=O>>[F:1][C:2]([F:10])([C:6]([F:9])([F:8])[F:7])[CH2:3][O:4][CH2:5][Cl:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 280Carbon DioxideHCID 24648Sulfuryl chlorideHCID 27760151,1,1,2,2-Pentafluoro-3-methoxypropane

生成物 1

HCID 215171363-(Chloromethoxy)-1,1,1,2,2-pentafluoropropane

反応条件

温度
33 °C

実験手順

Methyl 2,2,3,3,3-pentafluoropropyl ether (225g, 1.37 mole) in a flask fitted with a dry ice cooled condensor and moisture trap was stirred, heated to 33°C, irradiated with ultraviolet light, and sulfuryl chloride (174 g, 1.29 mole) was added dropwise. The reaction temperature dropped to about 0°C as SO2 returned from the condensor. The condensor was allowed to warm gradually to permit SO2 to escape and the reaction temperature to rise to about 33°C to complete the chlorination. The product was washed with ice cold water then with dilute sodium hydroxide solution to remove SO2 and dried to give 250 g of crude XXVII. This was fractionally distilled to give XXVII, b760 87.1-88.5; yield 159 g, purity 92% by GLC. The structure of XXVII was confirmed by proton NMR spectroscopy.

後処理

  1. additionwas added dropwise
  2. additionThe reaction temperature dropped to about 0°C as SO2
  3. temperatureto warm gradually
  4. customto rise to about 33°C
  5. washThe product was washed with ice cold water
  6. customwith dilute sodium hydroxide solution to remove SO2
  7. customdried

出典と根拠

ORDレコード
ord-f798dd15bbd84965b7208df5684f90f1
出典データセット
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03943256

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート