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Potassium Carbonate → HCID 68615140, 화합물

HRID 1841584
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HRID 1841584 반응식
[C:1]([O:5][C:6](=[O:16])[N:7]([C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1)[CH3:8])([CH3:4])([CH3:3])[CH3:2].C([O-])([O-])=O.[K+].[K+].[Br:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]Br>CC(C)=O>[C:1]([O:5][C:6](=[O:16])[N:7]([C:9]1[CH:10]=[CH:11][C:12]([O:15][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][Br:23])=[CH:13][CH:14]=1)[CH3:8])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 123681,6-DibromohexaneHCID 54592515(4-Hydroxy-phenyl)-methyl-carbamic acid tert-butyl ester

생성물 1

HCID 68615140HCID 68615140, 화합물수율 86.2%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A solution of 6.56 g (29.4 mmol) of (4-Hydroxy-phenyl)-methyl-carbamic acid tert-butyl ester dissolved in 250 ml of acetone was treated with 12.2 g (88.1 mmol) of K2CO3 and 13.4 ml (88.1 mmol) of 1,6-dibromohexane. The suspension was heated under reflux overnight, cooled, filtered and concentrated. Purification by flash chromatography on silica gel with toluene/EtOAc (95:5) as eluent yielded 9.79 g (86%) of [4-(6-Bromo-hexyloxy)-phenyl]-methyl-carbamic acid tert-butyl ester, MS: 386 (MH+, 1Br).

후처리

  1. temperatureThe suspension was heated
  2. temperatureunder reflux overnight
  3. temperaturecooled
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customPurification by flash chromatography on silica gel with toluene/EtOAc (95:5) as eluent

출처 및 근거

ORD 기록
ord-b3c7423172e44b07814dae21d1038fa9
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06683201B2

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