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N-bromobutanimide → cis-4-[4-Bromo-3-(2-methyl-3-furanyl)phenyl]-2,6-dimethylmorpholine

HRID 2278429
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인쇄 미리보기

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HRID 2278429 반응식
[Br:1]N1C(=O)CCC1=O.[CH3:9][C@H:10]1[O:15][C@@H:14]([CH3:16])[CH2:13][N:12]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([C:23]3[CH:27]=[CH:26][O:25][C:24]=3[CH3:28])[CH:18]=2)[CH2:11]1>C(Cl)(Cl)Cl>[Br:1][C:20]1[CH:21]=[CH:22][C:17]([N:12]2[CH2:11][C@H:10]([CH3:9])[O:15][C@H:14]([CH3:16])[CH2:13]2)=[CH:18][C:19]=1[C:23]1[CH:27]=[CH:26][O:25][C:24]=1[CH3:28]
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 67513891cis-2,6-Dimethyl-4-[3-(2-methyl-3-furanyl)phenyl]morpholine

생성물 1

HCID 69088074cis-4-[4-Bromo-3-(2-methyl-3-furanyl)phenyl]-2,6-dimethylmorpholine

시약·촉매·용매 1

HCID 6212Chloroform용매

반응 조건

온도
0 °C

실험 절차

N-Bromosuccinimide (380 mg, 2.137 mmol) was added portionwise to a solution of cis-2,6-dimethyl-4-[3-(2-methyl-3-furanyl)phenyl]morpholine (580 mg, 2.137 mmol) in chloroform (10 mL) at 0° C. The reaction was stirred at 0° C. for 1 hour. Crude LC/MS showed desired product can be seen and no starting material left, so the reaction mixture was diluted with ethyl acetate and washed with water, brine, water and brine. The organic layer was dried (sodium sulfate), filtered and concentrated under reduced pressure.

출처 및 근거

ORD 기록
ord-204d74eb663d4fe9b744762f9f63fd41
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133178B2

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