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

HRID 1601129
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HRID 1601129 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 335O-CresolHCID 24758Sodium hydride2회HCID 114264722-Iodobenzyl Bromide

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-05e04f26e13443a5b8b8da93c1b73283
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977149

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