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Dichloromethane → 4-(Chloromethyl)-2-(furan-2-yl)-5-methyl-1,3-oxazole

HRID 1182822
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반응식

HRID 1182822 반응식
Cl[CH2:2][Cl:3].[O:4]1[CH:8]=[CH:7][CH:6]=[C:5]1[C:9]1[O:10][C:11]([CH3:16])=[C:12](CO)[N:13]=1.C1(C)C=CC(S(Cl)(=O)=O)=CC=1>O>[Cl:3][CH2:2][C:12]1[N:13]=[C:9]([C:5]2[O:4][CH:8]=[CH:7][CH:6]=2)[O:10][C:11]=1[CH3:16]
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참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 73974-Toluenesulfonyl chlorideHCID 178612042-(2-Furyl)-5-methyl-4-oxazolylmethanol

생성물 1

HCID 223445824-(Chloromethyl)-2-(furan-2-yl)-5-methyl-1,3-oxazole수율 31%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The dichloromethane (1 mL) solution of {2-(furan-2-yl)-5-methyloxazol-4-yl}methanol (36 mg, 0.2 mmol), N,N-dimethylaminopyridine (37 mg, 0.3 mmol) and p-toluene sulfonyl chloride (57 mg, 0.3 mmol) was stirred at 60° C. for 2 hrs. The reaction mixture was added water and extracted with ethyl acetate. The organic layer was combined, washed with water and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resulting residues were subjected to silica gel column chromatography (hexane/ethyl acetate) to obtain 4-(chloromethyl)-2-(furan-2-yl)-5-methyloxazole (13 mg, 31%) as a transparent oil.

후처리

  1. extractionextracted with ethyl acetate
  2. washwashed with water and brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7fba429e75f04240aadfd731009a9fdb
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664226B2

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