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Isopropanol → 2-(2-Methoxyphenyl)cyclopentan-1-one

HRID 475863
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HRID 475863 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]1[CH2:13][CH2:12][CH2:11][CH:10]1[OH:14].CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C>CC(C)=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]1[CH2:13][CH2:12][CH2:11][C:10]1=[O:14]
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참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 12333721HCID 12333721, 화합물HCID 131709961Jones' reagent

생성물 1

HCID 123337222-(2-Methoxyphenyl)cyclopentan-1-one수율 73.6%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of 2-(2-methoxyphenyl)cyclopentanol (9.11 g, 47.4 mmol) in Acetone (Volume: 474 ml) was added Jones reagent (6.52 ml, 52.1 mmol) (8.0 M). After the addition was complete (the conversion of red reagent to green solid, and the supernatant solution took on the color of unreacted reagent), isopropanol was added to quench the excess reagent. The green solid was filtered off through ceilite and rinsed with acetone. The filtrate was concentrated and purified by flash chromatography to get 2-(2-methoxyphenyl)cyclopentanone (6.64 g, 34.9 mmol, 73.6% yield). LC-MS (M+H)+=191.0. 1H NMR (500 MHz, CD3OD) δ 7.24 (td, J=7.8, 1.8 Hz, 1H), 7.09 (dd, J=7.5, 1.7 Hz, 1H), 6.95 (d, J=8.2 Hz, 1H), 6.90 (td, J=7.4, 1.1 Hz, 1H), 3.77 (s, 3H), 3.43-3.37 (m, 1H), 2.48-2.30 (m, 3H), 2.23-2.11 (m, 2H), 2.00-1.88 (m, 1H).

후처리

  1. additionAfter the addition
  2. additionwas added
  3. customto quench the excess reagent
  4. filtrationThe green solid was filtered off through ceilite
  5. washrinsed with acetone
  6. concentrationThe filtrate was concentrated
  7. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-9d0aa32e73f24259beef781e4627c39e
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637525B2

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