Pyridine → HCID 11256949、化合物

HRID 1602753ノート

反応式

HRID 1602753 の反応式
[C:1](Cl)(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH3:7][Si:8]([Si:11]([Si:19]([CH3:22])([CH3:21])[CH3:20])([Si:15]([CH3:18])([CH3:17])[CH3:16])[CH2:12][CH2:13][OH:14])([CH3:10])[CH3:9].N1C=CC=CC=1>O1CCCC1.C1C2NC3C(=CC=CC=3)SC=2C=CC=1>[C:1]([O:14][CH2:13][CH2:12][Si:11]([Si:19]([CH3:22])([CH3:21])[CH3:20])([Si:15]([CH3:18])([CH3:17])[CH3:16])[Si:8]([CH3:7])([CH3:9])[CH3:10])(=[O:5])[C:2]([CH3:4])=[CH2:3]

参加物

6

反応物 3

HCID 1049PyridineHCID 13528Methacryloyl chlorideHCID 133081222-[1,1,1,3,3,3-Hexamethyl-2-(trimethylsilyl)trisilan-2-yl]ethan-1-ol

生成物 1

HCID 11256949HCID 11256949、化合物収率 63%

試薬・触媒・溶媒 2

HCID 7108Phenothiazine触媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Methacryloyl chloride (2.50 grams, 0.024 mole) in 25 ml tetrahydro-furan was added dropwise into a solution of 2-tris(trimethylsilyl) silyl ethanol (6.5 grams, 0.022 mole), pyridine (2.0 grams, 0.025 mole) and 25 mg of phenothiazine in 50 ml tetrahydrofuran at room temperature. Stirred at room temperature for two more hours. The solids were filtered off and the solution was washed with 100 ml brine. The solution was then diluted with 100 ml ether and washed with 5% hydrochloric acid, followed by deionzed water, and then with brine. It was dried over anhydrous magnesium sulfate and was concentrated in vacuo. Fractional distillation under reduced pressed gave 5 grams of the product at 105-115° C. at 0.5 mm.

後処理

  1. filtrationThe solids were filtered off
  2. washthe solution was washed with 100 ml brine
  3. additionThe solution was then diluted with 100 ml ether
  4. washwashed with 5% hydrochloric acid
  5. dry with materialIt was dried over anhydrous magnesium sulfate
  6. concentrationwas concentrated in vacuo
  7. distillationFractional distillation

出典と根拠

ORDレコード
ord-66f14550627c402099b9e1e3563baa38
出典データセット
uspto-grants-1999_11
特許番号
US05985524

反応ノート

読み込み中…