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(Diethylamino)sulfur trifluoride → HCID 86646156、化合物

HRID 551690
ノート
印刷プレビュー

反応式

HRID 551690 の反応式
O[CH2:2][CH2:3][CH:4]([CH2:12][CH:13]=[CH2:14])/[CH:5]=[CH:6]/[C:7]([O:9][CH2:10][CH3:11])=[O:8].CCN(S(F)(F)[F:21])CC.C(=O)(O)[O-].[Na+]>O1CCCC1>[F:21][CH2:2][CH2:3][CH:4]([CH2:12][CH:13]=[CH2:14])/[CH:5]=[CH:6]/[C:7]([O:9][CH2:10][CH3:11])=[O:8]
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 123472(Diethylamino)sulfur trifluorideHCID 516892Sodium BicarbonateHCID 86646155HCID 86646155、化合物

生成物 1

HCID 86646156HCID 86646156、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Ethyl(E)-4-(2-hydroxyethyl)-hepta-2,6-dienoate (5 g, 27.1 mmol) was dissolved in tetrahydrofuran (40 mL). To the solution, DAST (4.8 g, 29.8 mmol) was added under ice cooling, and the mixture was stirred for 1 hour. The reaction solution was poured to a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with saturated saline, then dried, and then concentrated. The residue was purified by silica gel column chromatography (200 g) to obtain the compound of interest as an oil substance (2.2 g, 44%).

後処理

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe ethyl acetate layer was washed with saturated saline
  3. customdried
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel column chromatography (200 g)
  6. customto obtain the compound of interest as an oil substance (2.2 g, 44%)

出典と根拠

ORDレコード
ord-1842d5e3a2244ce7a6e4fa78749afee2
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07947738B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート