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Triacetoxyperiodinane → 2-Bromo-3,4-difluorobenzaldehyde

HRID 63690
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HRID 63690 반응식
[Br:1][C:2]1[C:7]([F:8])=[C:6]([F:9])[CH:5]=[CH:4][C:3]=1[CH2:10][OH:11].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>ClCCl.CCOC(C)=O.C(Cl)Cl>[Br:1][C:2]1[C:7]([F:8])=[C:6]([F:9])[CH:5]=[CH:4][C:3]=1[CH:10]=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 159087TriacetoxyperiodinaneHCID 69798476(2-Bromo-3,4-difluorophenyl)methanol

생성물 1

HCID 577551402-Bromo-3,4-difluorobenzaldehyde수율 119.1%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 21226138Dichloromethane ethylacetate용매

실험 절차

(2-Bromo-3,4-difluorophenyl)methanol (Compound AR) (2.55 g, 11.4 mmol, Eq: 1.00) was dissolved in dichloromethane (15 ml). Dess-Martin periodinane (4.85 g, 11.4 mmol, Eq: 1.00) was added. The reaction mixture was stirred for 2 hrs at room temperature. The reaction mixture was filtered over a plug of celite and washed with DCM (30 ml). Filtrate was concentrated to give a semi solid. Crude product was dissolved in EtOAc/DCM and loaded into a silica gel column (4 g). Silica gel column was flushed with EtOAc to give a light yellow solid (3 g). 1H NMR (DMSO) δ 10.13 (s, 1H), 7.74-7.82 (m, 1H), 7.70 (ddd, J=9.5, 7.3, 0.8 Hz, 1H).

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후처리

  1. filtrationThe reaction mixture was filtered over a plug of celite
  2. washwashed with DCM (30 ml)
  3. concentrationFiltrate was concentrated
  4. customto give a semi solid
  5. customSilica gel column was flushed with EtOAc

출처 및 근거

ORD 기록
ord-f7375c218ef149f2866251ce8258f819
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447086B2

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