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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Trimethyl borate → Boric Acid

HRID 1452445
ノート
印刷プレビュー

反応式

HRID 1452445 の反応式
[B:1]([O:6][CH3:7])([O:4][CH3:5])[O:2][CH3:3].C(O)(=O)C(C)=C.CC(O)COC(CO)C>>[B:1]([OH:6])([OH:4])[OH:2].[B:1]([O:6][CH3:7])([O:4][CH3:5])[O:2][CH3:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8470Trimethyl borateHCID 86592450HCID 86592450、化合物

生成物 2

HCID 7628Boric AcidHCID 8470Trimethyl borate

反応条件

温度
60 °C

実験手順

207.6 Grams (2.0 mols) of trimethyl borate was added to 606 g (3.0 mols) of dipropylene glycol monomethacrylate. The mixture was heated to 60° C. with stirring in a dry air atmosphere. The mixture was kept at 60° C. for 1 hour, followed by heating to 75° C. After the temperature reached 75° C., the pressure in the system was gradually reduced. The system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours to remove volatile matters produced with progress of ester interchange reaction of boric acid and excess trimethyl borate, followed by filtration to obtain 600 g of a polymerizable boron-containing compound F (an esterification product of boric acid with dipropylene glycol monomethacrylate) represented by the formula (2). An infrared absorption spectrum of the resulting polymerizable boron-containing compound F was measured to confirm that the absorption band originating from hydroxyl group at 3300 cm−1 disappeared.

後処理

  1. temperatureby heating to 75° C
  2. customreached 75° C.
  3. waitThe system was kept at a pressure of 2.67 kPa (20 mmHg) or lower for 6 hours
  4. customto remove volatile matters

出典と根拠

ORDレコード
ord-93cdc2e060a5412583d6c29c87560b34
出典データセット
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07473492B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート