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Allyl bromide → Methyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylate

HRID 2248288
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HRID 2248288 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH2:7][CH2:6][CH:5]2[C:12]([O:14][CH3:15])=[O:13].[H-].[Na+].[CH2:18](Br)[CH:19]=[CH2:20].[Cl-].[NH4+]>CN(C)C=O>[F:1][C:2]1[CH:11]=[CH:10][C:9]2[O:8][CH2:7][CH2:6][C:5]([CH2:20][CH:19]=[CH2:18])([C:12]([O:14][CH3:15])=[O:13])[C:4]=2[CH:3]=1
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참가 물질

6

반응물 4

HCID 7841Allyl bromideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 14986536Methyl 6-fluorochromane-4-carboxylate

생성물 1

HCID 19094435Methyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylate

시약·촉매·용매 1

HCID 6228Dimethylformamide
용매
2회

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온도
0 °C

실험 절차

A solution of methyl 6-fluorochromane-4-carboxylate (2.1 g) in anhydrous N,N-dimethylformamide was added to a suspension of sodium hydride (265 mg) in anhydrous N,N-dimethylformamide under nitrogen. After gas evolution ceased, the mixture was cooled to 0° C., and neat allyl bromide (0.95 mL) was added. After 1 hour, 20 mL of an aqueous saturated ammonium chloride solution was added, and the mixture extracted with ethyl acetate, the extracts washed with water, brine, dried over anhydrous sodium sulfate, filtered and evaporated to afford the title compound as a colorless oil, 2.4 g. (HRMS calc'd 250.1004; found 250.1002).

후처리

  1. extractionthe mixture extracted with ethyl acetate
  2. washthe extracts washed with water, brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. customevaporated

출처 및 근거

ORD 기록
ord-1e8e33b6c94b4215bb212e3439e4d1e7
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05039672

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