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Epichlorohydrin → 2-[(2-Iodophenoxy)methyl]oxirane

HRID 1906510
ノート
印刷プレビュー

反応式

HRID 1906510 の反応式
[H-].[Na+].[I:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10].[CH2:11]([CH:13]1[O:15][CH2:14]1)Cl>>[I:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][CH2:11][CH:13]1[CH2:14][O:15]1
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 7835EpichlorohydrinHCID 107842-IodophenolHCID 24758Sodium hydride

生成物 1

HCID 130640342-[(2-Iodophenoxy)methyl]oxirane収率 80%

反応条件

温度
70 °C

実験手順

To a round bottom flask under N2 was added 4.56 g (0.095 mole) of 50% NaH in oil. The NaH was washed twice with hexane, then 220 ml of DMF was added. Aliquots of 20.0 g (0.091 mole) of o-iodophenol were added over 15 minutes then 30.0 ml (0.450 mole) of epichlorohydrin was added and the solution heated to 70° C. After two hours the reaction was evaporated in vacuo, taken into CHCl3, washed with 10% NaOH, water, and brine and dried with MgSO4. The solvent was evaporated in vacuo to give 24.93 g of crude product. Distillation at 110°-114° C., 0.05 mm Hg gave 20.0 g (80.0%) of [(2-iodophenoxy)methyl]oxirane.

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

後処理

  1. washThe NaH was washed twice with hexane
  2. addition220 ml of DMF was added
  3. customAfter two hours the reaction was evaporated in vacuo
  4. washwashed with 10% NaOH, water, and brine
  5. dry with materialdried with MgSO4
  6. customThe solvent was evaporated in vacuo
  7. customto give 24.93 g of crude product
  8. distillationDistillation at 110°-114° C.

出典と根拠

ORDレコード
ord-061404c5f26b45a4beaa0c447ab4a4b3
出典データセット
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04652584

反応ノート

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