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Anisole → Cyclobutyl(4-methoxyphenyl)methanone

HRID 645337
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HRID 645337 반응식
[Al+3].[Cl-].[Cl-].[Cl-].[CH:5]1([C:9]([OH:11])=O)[CH2:8][CH2:7][CH2:6]1.[C:12]1([O:18][CH3:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>[N+](CC)([O-])=O>[CH:5]1([C:9]([C:15]2[CH:16]=[CH:17][C:12]([O:18][CH3:19])=[CH:13][CH:14]=2)=[O:11])[CH2:6][CH2:7][CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7519AnisoleHCID 19494Cyclobutanecarboxylic acidHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 13813654Cyclobutyl(4-methoxyphenyl)methanone

시약·촉매·용매 1

HCID 6587Nitroethane용매2회

실험 절차

A solution of AlCl3 (13.4 g) in nitroethane (25 ml) was added to a solution of cyclobutane carboxylic acid (10.0 g) and anisole (10.8 g) in nitroethane (75 ml) at 10° C. The mixture was stirred for 5 hours at room temperature, was than poured on ice and extracted with MTBE. The organic phase was washed with aqueous sodium hydroxide, water and brine, dried (MgSO4) and concentrated in vacuo. The essentially clean ketone (10.8 g) was used in the next step.

후처리

  1. additionthan poured on ice
  2. extractionextracted with MTBE
  3. washThe organic phase was washed with aqueous sodium hydroxide, water and brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3261a68a68b9411693b7b568306ab53e
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07704942B2

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