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Methacrylic Acid → (2-Adamantyloxymethyl)methacrylate

HRID 1716170
ノート
印刷プレビュー

反応式

HRID 1716170 の反応式
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].C(N(CC)CC)C.Cl[CH2:15][O:16][CH:17]1[CH:24]2[CH2:25][CH:20]3[CH2:21][CH:22]([CH2:26][CH:18]1[CH2:19]3)[CH2:23]2>O1CCCC1>[CH:18]12[CH2:26][CH:22]3[CH2:21][CH:20]([CH2:25][CH:24]([CH2:23]3)[CH:17]1[O:16][CH2:15][O:5][C:1](=[O:6])[C:2]([CH3:4])=[CH2:3])[CH2:19]2
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 4093Methacrylic AcidHCID 8471TriethylamineHCID 10932491HCID 10932491、化合物

生成物 1

HCID 23150858(2-Adamantyloxymethyl)methacrylate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

6.9 g of methacrylic acid was dissolved in 200 ml of tetrahydrofuran, and 8.0 g of triethylamine was added. Following stirring at room temperature, a solution containing 15 g of 2-adamantyl chloromethyl ether dissolved in 100 ml of tetrahydrofuran was added dropwise to the reaction solution. Following stirring for 12 hours at room temperature, the precipitated salt was removed by filtration. The solvent was removed from the remaining filtrate by evaporation, the residue was dissolved in 200 ml of ethyl acetate, and following washing with pure water (100 ml×3), the solvent was removed by evaporation. The residue was then allowed to stand under ice cooling, thereby yielding a white solid.

後処理

  1. additionwas added dropwise to the reaction solution
  2. stirringFollowing stirring for 12 hours at room temperature
  3. customthe precipitated salt was removed by filtration
  4. customThe solvent was removed from the remaining filtrate by evaporation
  5. dissolutionthe residue was dissolved in 200 ml of ethyl acetate
  6. washfollowing washing with pure water (100 ml×3)
  7. customthe solvent was removed by evaporation
  8. customyielding a white solid

出典と根拠

ORDレコード
ord-5c70ff849142413b982041e4b5459fee
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07803512B2

反応ノート

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