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Iodine → 4-Benzyloxy-2-iodo-5-methoxybenzaldehyde

HRID 2075943
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반응식

HRID 2075943 반응식
[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=[O:14])=[CH:11][C:10]=1[O:17][CH3:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I:19]I>FC(F)(F)C([O-])=O.[Ag+].C(Cl)Cl>[CH2:1]([O:8][C:9]1[C:10]([O:17][CH3:18])=[CH:11][C:12]([CH:13]=[O:14])=[C:15]([I:19])[CH:16]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 807IodineHCID 755064-(Benzyloxy)-3-methoxybenzaldehyde

생성물 1

HCID 127730874-Benzyloxy-2-iodo-5-methoxybenzaldehyde수율 86.9%

시약·촉매·용매 2

HCID 76299Silver trifluoroacetate촉매HCID 6344Dichloromethane용매

실험 절차

To a mixture of 4-benzyloxy-3-methoxybenzaldehyde (10 g), silver trifluoroacetate (11.4 g) and methylene chloride (105 mL) was added iodine (13.1 g) at room temperature. After stirring for 2 hours, the mixture was passed through a layer of Celite (registered mark). The filtrate was washed with an aqueous solution of sodium hydrogen sulfite and brine successively, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was triturated with methanol:water=4:1 to give the title compound (13.2 g).

후처리

  1. washThe filtrate was washed with an aqueous solution of sodium hydrogen sulfite and brine successively
  2. dry with materialdried over anhydrous magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was triturated with methanol

출처 및 근거

ORD 기록
ord-cfb742ef909f45e0959cca8f21986bd4
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07923462B2

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