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O-Cresol → 1-Iodo-2-[(2-methylphenoxy)methyl]benzene

HRID 1601129
ノート
印刷プレビュー

反応式

HRID 1601129 の反応式
[H-].[Na+].[C:3]1([CH3:10])[C:8]([OH:9])=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[I:19]>O1CCCC1>[I:19][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[CH2:12][O:9][C:8]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:10]
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

5

反応物 3

HCID 335O-CresolHCID 24758Sodium hydride2 回HCID 114264722-Iodobenzyl Bromide

生成物 1

HCID 193600291-Iodo-2-[(2-methylphenoxy)methyl]benzene収率 94%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

Sodium hydride (60% oil dispersion) (7.8 g) was added portionwise to a ice-water cooled solution of o-cresol (21.1 g) in tetrahydrofuran (500 mL). The mixture was stirred 20 minutes and then 1-(bromomethyl)-2-iodobenzene (58 g) was added. The mixture was warmed to 60° C. for 16 h. Additional sodium hydride (2 g) was added and the reaction mixture heated for an additional 3 h. The reaction mixture was cooled and carefully quenched with water and extracted with ethyl acetate (2×250 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure to an oil, which was triturated with cold hexane to provide a solid which was collected by filtration to yield 59.1 g (94%) of the title compound of Step B as a white solid, mp 106-108° C.

後処理

  1. temperaturethe reaction mixture heated for an additional 3 h
  2. temperatureThe reaction mixture was cooled
  3. customcarefully quenched with water
  4. extractionextracted with ethyl acetate (2×250 mL)
  5. dry with materialThe combined organic extracts were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure to an oil, which
  8. customwas triturated with cold hexane
  9. customto provide a solid which
  10. filtrationwas collected by filtration

出典と根拠

ORDレコード
ord-05e04f26e13443a5b8b8da93c1b73283
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05977149

反応ノート

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