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Methanol → Methyl 2-(4-Bromophenoxymethyl)benzoic Acid

HRID 1515223
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HRID 1515223 반응식
[OH-].[Na+].[Br:3][C:4]1[CH:21]=[CH:20][C:7]([O:8][CH2:9][C:10]2[CH:19]=[CH:18][CH:17]=[CH:16][C:11]=2[C:12]([O:14]C)=[O:13])=[CH:6][CH:5]=1.[CH3:22]O>>[CH3:22][C:19]1[C:10]([CH2:9][O:8][C:7]2[CH:20]=[CH:21][C:4]([Br:3])=[CH:5][CH:6]=2)=[C:11]([CH:16]=[CH:17][CH:18]=1)[C:12]([OH:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 53995976Methyl 2-((4-bromophenoxy)methyl)benzoate

생성물 1

HCID 68526746Methyl 2-(4-Bromophenoxymethyl)benzoic Acid수율 84%

실험 절차

A 2 mol/L aqueous sodium hydroxide solution (250 mL) was added to a methanol (1 L) solution of methyl 2-(4-bromophenoxymethyl)-benzoate (139 g, 432 mmol), and the mixture was stirred overnight while heating under reflux. Methanol was distilled off under a reduced pressure, and a 6 mol/L hydrochloric acid was added to the residue obtained to precipitate the crystals, and the precipitated crystals were collected by filtration, and sufficiently washed with water. The crystals were dried over phosphorus pentoxide at 50° C., to give 112 g (84%) of the captioned compound.

후처리

  1. temperaturewhile heating
  2. temperatureunder reflux
  3. distillationMethanol was distilled off under a reduced pressure
  4. additiona 6 mol/L hydrochloric acid was added to the residue
  5. customobtained
  6. customto precipitate the crystals
  7. filtrationthe precipitated crystals were collected by filtration
  8. washsufficiently washed with water
  9. dry with materialThe crystals were dried over phosphorus pentoxide at 50° C.

출처 및 근거

ORD 기록
ord-d032d885cf694bdf85fbc0952f03b1c6
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222419B2

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