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Methylparaben → methyl 4-(oxiran-2-ylmethoxy)benzoate

HRID 2166514
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HRID 2166514 반응식
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:18]([CH:20]1[O:22][CH2:21]1)Cl>CC(C)=O>[O:22]1[CH2:21][CH:20]1[CH2:18][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7456MethylparabenHCID 7835EpichlorohydrinHCID 11430Potassium Carbonate

생성물 1

HCID 2771933methyl 4-(oxiran-2-ylmethoxy)benzoate수율 67.2%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of 15.2 gm (0.1 mole) of methyl 4-hydroxybenzoate, 27.6 gm (0.2 mole) potassium carbonate and 31 mL (0.4 mole) epichlorohydrin in 250 mL acetone was heated to reflux for 24 hours. The reaction medium was then filtered and evaporated. The residue was taken up in 100 mL toluene and washed with 100 mL 1.0 N NaOH and 2×100 mL water. The toluene phase was then dried over magnesium sulfate and evaporated to provide the crude product as an oil. Purification was effected by vacuum distillation (66°-67°; 75 u pressure) and provided 14 gm (67%) of a clear oil when gradually crystallized at room temperature: mp 54°-55° C. The NMR and IR spectra and elemental analysis data were consistent with the assigned structure.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 24 hours
  3. filtrationThe reaction medium was then filtered
  4. customevaporated
  5. washwashed with 100 mL 1.0 N NaOH and 2×100 mL water
  6. dry with materialThe toluene phase was then dried over magnesium sulfate
  7. customevaporated
  8. customto provide the crude product as an oil
  9. customPurification
  10. distillationwas effected by vacuum distillation (66°-67°; 75 u pressure)

출처 및 근거

ORD 기록
ord-b06ff2a8f24b4e8f8f34ca2f104c3742
출처 데이터셋
uspto-grants-1983_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04387103

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