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2-(3-Chloropropyl)-2-methyl-1,3-dioxolane → 2-(3-Bromopropyl)-2-methyl-1,3-dioxolane

HRID 1680096
ノート
印刷プレビュー

反応式

HRID 1680096 の反応式
[CH2:1]1[O:10][C:4]([CH2:6][CH2:7][CH2:8]Cl)([CH3:5])[O:3][CH2:2]1.[Br-:11].[Li+].C(N(C(C)C)CC)(C)C>O1CCCC1>[CH2:1]1[O:10][C:4]([CH2:6][CH2:7][CH2:8][Br:11])([CH3:5])[O:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 800792-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 81531DiisopropylethylamineHCID 82050Lithium Bromide

生成物 1

HCID 5600542-(3-Bromopropyl)-2-methyl-1,3-dioxolane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

4.0 Parts of 5-chloro-2-pentanone ethylene ketal is mixed with 9.0 parts of lithium bromide and 2.0 parts of diisopropylethylamine in 30 parts by volume of tetrahydrofuran which has been distilled from lithium aluminum hydride. The mixture is refluxed under nitrogen for 48 hours, cooled and poured into a mixture of ether and water for extraction. The ether layer is washed twice with water, then with 1 N hydrochloric acid and then twice again with water. The ether layer is then dried over sodium sulfate and evaporated under reduced pressure to give 5-bromo-2-pentanone ethylene ketal having the formula ##STR6##

後処理

  1. distillationhas been distilled from lithium aluminum hydride
  2. temperatureThe mixture is refluxed under nitrogen for 48 hours
  3. temperaturecooled
  4. additionpoured into a mixture of ether and water for extraction
  5. washThe ether layer is washed twice with water
  6. dry with materialThe ether layer is then dried over sodium sulfate
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-5af8367d6c97437fbedeab8b39088a6f
出典データセット
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04271314

反応ノート

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