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Methyl Acrylate → Methyl (E)-3-(6-heptyloxynaphth-2-yl)acrylate

HRID 650850
ノート
印刷プレビュー

反応式

HRID 650850 の反応式
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[CH:6]=[CH:5]2.[C:20]([O:24][CH3:25])(=[O:23])[CH:21]=[CH2:22].C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(N(CC)CC)C>[CH2:13]([O:12][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[CH:3]=[C:2](/[CH:22]=[CH:21]/[C:20]([O:24][CH3:25])=[O:23])[CH:11]=[CH:10]2)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 7294Methyl AcrylateHCID 80271Tri-o-tolylphosphineHCID 106157136-Bromo-2-heptyloxynaphthalene

生成物 1

HCID 21182539Methyl (E)-3-(6-heptyloxynaphth-2-yl)acrylate

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 8471Triethylamine溶媒

実験手順

A mixture of 5.2 g of 6-bromo-2-heptyloxynaphthalene, 25 ml of triethylamine, 4.3 ml of methyl acrylate, 0.072 g of palladium acetate and 0.392 g of tri-o-tolylphosphine is refluxed for 16 hours. The reaction mixture is then cooled and is partitioned between ethyl acetate and water and the organic phase is washed with water, dried over magnesium sulfate, filtered and evaporated down. The residue is chromatographed over 250 g of silica gel using toluene/ethyl acetate (3:1) and then crystallized from toluene. This gives methyl (E)-3-(heptyloxynaphth-2-yl)acrylate.

後処理

  1. temperatureis refluxed for 16 hours
  2. temperatureThe reaction mixture is then cooled
  3. customis partitioned between ethyl acetate and water
  4. washthe organic phase is washed with water
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated down
  8. customThe residue is chromatographed over 250 g of silica gel
  9. customcrystallized from toluene

出典と根拠

ORDレコード
ord-66da3151daeb4fe9bf4d1e312a52499b
出典データセット
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06277502B1

反応ノート

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