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Water → Methyl 2-(prop-2-en-1-yloxy)benzoate

HRID 1107539
ノート
印刷プレビュー

反応式

HRID 1107539 の反応式
[CH2:1](Br)[CH:2]=[CH2:3].[C:5]([O:14][CH3:15])(=[O:13])[C:6]1[C:7](=[CH:9][CH:10]=[CH:11][CH:12]=1)[OH:8].C(=O)([O-])[O-].[K+].[K+].O>C1COCC1.CN(C=O)C>[CH2:1]([O:8][C:7]1[CH:9]=[CH:10][CH:11]=[CH:12][C:6]=1[C:5]([O:14][CH3:15])=[O:13])[CH:2]=[CH2:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 4133Methyl SalicylateHCID 7841Allyl bromideHCID 11430Potassium Carbonate

生成物 1

HCID 221897Methyl 2-(prop-2-en-1-yloxy)benzoate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8028Tetrahydrofuran

実験手順

A mixture of allyl bromide (152.4 g, 1.27 mol), methyl salicylate (162.44 g, 1.06 mol), and potassium carbonate (219.75 g, 1.59 mol) in THF (600 ml) and DMF (600 ml) was heated to reflux for 6 hr. The mixure was poured into water (3 L) and extracted with ethyl acetate three times. The ethyl acetate extracts were combined and washed with water and dried with brine. The ethyl acetate extracts were concentrated in vacuo to a yellow oil that was vacuum distilled to a clear oil (163.45 g, 80%).

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 6 hr
  3. extractionextracted with ethyl acetate three times
  4. washwashed with water
  5. dry with materialdried with brine
  6. concentrationThe ethyl acetate extracts were concentrated in vacuo to a yellow oil that
  7. distillationdistilled to a clear oil (163.45 g, 80%)

出典と根拠

ORDレコード
ord-daa66a336b9a4fa6bb688c4c67682299
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06060506

反応ノート

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