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Benzyl Bromide → Methyl 2-hydroxy-3-propyl-4-benzyloxybenzoate

HRID 2289087
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HRID 2289087 반응식
[OH:1][C:2]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10]([OH:15])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[CH2:16](Br)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[OH:1][C:2]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 13019281Methyl 2,4-dihydroxy-3-propylbenzoate

생성물 1

HCID 18701907Methyl 2-hydroxy-3-propyl-4-benzyloxybenzoate

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

A solution of methyl 2,4-dihydroxy-3-propylbenzoate (3.00 grams) in 2-butanone (30 mL) was treated with benzyl bromide (1.70 mL) and potassium carbonate (1.972 grams). The mixture was refluxed for 4 hours. The reaction mixture was partitioned between isopropyl acetate and pH 4 buffer. The organic was washed once with water, then dried over magnesium sulfate. The organic was filtered and evaporated to an oil which was chromatographed over silica gel to afford the title compound.

후처리

  1. temperatureThe mixture was refluxed for 4 hours
  2. customThe reaction mixture was partitioned between isopropyl acetate and pH 4 buffer
  3. washThe organic was washed once with water
  4. dry with materialdried over magnesium sulfate
  5. filtrationThe organic was filtered
  6. customevaporated to an oil which
  7. customwas chromatographed over silica gel

출처 및 근거

ORD 기록
ord-900c89412cd34dd0b52e12659f399e85
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06090836

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