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Diethyl Ether → 2-(5-Bromo-2-methoxyphenyl)propan-2-ol

HRID 2182648
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HRID 2182648 반응식
[CH3:1][Mg]Br.COC(=O)[C:7]1[CH:12]=[C:11]([Br:13])[CH:10]=CC=1OC.[CH2:17]([O:19][CH2:20][CH3:21])C.[Cl-].[NH4+].[O:24]1[CH2:28][CH2:27]CC1>C(OCC)(=O)C>[Br:13][C:11]1[CH:12]=[CH:7][C:20]([O:19][CH3:17])=[C:21]([C:28]([CH3:27])([OH:24])[CH3:1])[CH:10]=1
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참가 물질

7

반응물 5

HCID 3283Diethyl EtherHCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 13297188Methyl 5-bromo-2-methoxybenzoateHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 219488782-(5-Bromo-2-methoxyphenyl)propan-2-ol

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

실험 절차

62 ml of a 3 M methylmagnesium bromide solution in tetrahydrofuran is added in drops within one hour at 0 C. into 18.6 g of 5-bromo-2-methoxybenzoic acid methyl ester and 180 ml of diethyl ether. After 16 hours at room temperature and while being cooled with ice, it is mixed with saturated ammonium chloride solution and ethyl acetate. The ethyl acetate phase is washed with water, dried (Na2SO4) and concentrated by evaporation. After bulb tube distillation (boiling point: 140° C./0.04 hPa), 16.7 g of crystalline 1-(5-bromo-2-methoxyphenyl)-1-methylethanol is obtained. Flash point: 66-68° C.

후처리

  1. temperaturewhile being cooled with ice, it
  2. washThe ethyl acetate phase is washed with water
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated by evaporation
  5. distillationAfter bulb tube distillation (boiling point: 140° C./0.04 hPa)

출처 및 근거

ORD 기록
ord-7bc19cae3c9b4982b1172e2c0f23e922
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06897224B2

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