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Stearyl Alcohol → HCID 19593947, 화합물

HRID 612341
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HRID 612341 반응식
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[CH:20](N(C(C)C)CC)(C)C.FC(F)(F)S(OS(C(F)(F)F)(=O)=O)(=O)=O.[C:44]1([C:50]2[CH:51]=[CH:52][C:53]3[O:57][CH:56]=[N:55][C:54]=3[CH:58]=2)[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1>C(Cl)(Cl)Cl>[CH2:20]=[C:56]1[N:55]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:54]2[CH:58]=[C:50]([C:44]3[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=3)[CH:51]=[CH:52][C:53]=2[O:57]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8221Stearyl AlcoholHCID 67749Trifluoromethanesulfonic anhydrideHCID 81531DiisopropylethylamineHCID 33092485-phenylbenzoxazole

생성물 1

HCID 19593947HCID 19593947, 화합물수율 77%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

Powdered 1-octadecanol (15.4 g, 56.9 mmol) and diisopropylethylamine (9.9 mL, 56.9 mmol) are dissolved in 200 mL CHCl3 (dried over molecular sieves). To the above stirred solution is added trifluoromethanesulfonic anhydride (10.4 mL) dropwise over a period of 1 hours. Powdered 5-phenylbenzoxazole (16.7 g, 79.7 mmol) is then added portion-wise over a period of 10 minutes. After stirring overnight, the solution is washed with water and dried with anhydrous Na2SO4. The solution is loaded onto a large silica column and eluted with MeOH/CHCl3. The product is obtained as a colorless solid (20 g, 77%).

후처리

  1. washthe solution is washed with water
  2. dry with materialdried with anhydrous Na2SO4
  3. washeluted with MeOH/CHCl3

출처 및 근거

ORD 기록
ord-aed24100fa3d42ac8f9dbd85f7f67011
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06004536

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