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

HRID 1981644
ノート
印刷プレビュー

反応式

HRID 1981644 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7456MethylparabenHCID 7835EpichlorohydrinHCID 11430Potassium Carbonate

生成物 1

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

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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 1.0N 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.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 24 hours
  3. filtrationThe reaction medium was then filtered
  4. customevaporated
  5. washwashed with 100 mL 1.0N 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)

出典と根拠

ORDレコード
ord-9a9a168d71224b78ace01aa145a9e338
出典データセット
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04593119

反応ノート

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