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N-bromobutanimide → 2-(Bromomethyl)-5-(2'-methoxy-5'-fluorophenethyl)tetrahydrofuran

HRID 1919516
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반응식

HRID 1919516 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:4]=1[CH2:10][CH2:11][CH:12]([OH:17])[CH2:13][CH:14]=[CH:15][CH3:16].[Br:18]N1C(=O)CCC1=O>C(Cl)Cl>[Br:18][CH2:16][CH:15]1[CH2:14][CH2:13][CH:12]([CH2:11][CH2:10][C:4]2[CH:5]=[C:6]([F:9])[CH:7]=[CH:8][C:3]=2[O:2][CH3:1])[O:17]1
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 674997401-(5-Fluoro-2-methoxyphenyl)hept-5-en-3-ol

생성물 1

HCID 674993232-(Bromomethyl)-5-(2'-methoxy-5'-fluorophenethyl)tetrahydrofuran

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 1-(2′-methoxy-5′-fluorophenyl)hept-5-en-3-ol (3.5 g, 14.7 mmol) in dry CH2Cl2 (90 mL) at 0° C. was added N-bromosuccinimide (NBS, 3.15 g, 17.0 mmol) portionwise and the reaction was warmed to room temperature for 12 h. Solvent was then removed in vacuo and the residue was purified by flash column chromatography (5% EtOAc in Hexane, Rf=0.12) to result in the trans isomer (2.05 g, 44%) as an oil; and the cis isomer (743 mg, 16%) as an oil; and mixture of both isomers (1.35 g, 29%).

후처리

  1. customSolvent was then removed in vacuo
  2. customthe residue was purified by flash column chromatography (5% EtOAc in Hexane, Rf=0.12)
  3. customto result in the trans isomer (2.05 g, 44%) as an oil
  4. additionand mixture of both isomers (1.35 g, 29%)

출처 및 근거

ORD 기록
ord-bd272b23401f474f8bf54dfa10281f29
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08168635B2

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