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Nitrogen → HCID 53689240、化合物

HRID 1754994
ノート
印刷プレビュー

反応式

HRID 1754994 の反応式
CC1(C)N([O])C(C)(C)CCC1.C(OI(C1C=CC=CC=1)OC(=O)C)(=O)C.[F:27][C:28]([F:38])([F:37])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][OH:36].N#N>ClCCl>[F:27][C:28]([F:37])([F:38])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH:35]=[O:36]
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

6

反応物 4

HCID 947NitrogenHCID 76724Iodobenzene diacetateHCID 2724126TempoHCID 866727728,8,8-Trifluoro-octanol

生成物 1

HCID 53689240HCID 53689240、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

2,2,6,6-Tetramethylpiperidine 1-oxyl (202 mg, 1.29 mmol) and (diacetoxyiodo)benzene (3.33 g, 10.4 mmol) were added to a solution of 8,8,8-trifluoro-octanol (˜8.63 mmol) in dichloromethane (34.5 mL) at 0° C. in an N2 atmosphere, and the mixture was stirred at 0° C. for five minutes and at room temperature for 1.5 hours. The reaction solution was diluted with dichloromethane (200 mL), and the organic layer was sequentially washed with a saturated aqueous sodium sulfite solution (100 mL), a saturated aqueous sodium bicarbonate solution (100 mL) and saturated brine (100 mL). The organic layer was dried over sodium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 8,8,8-trifluoro-octanal as a colorless oily substance (310 mg, two steps, 20%).

後処理

  1. washthe organic layer was sequentially washed with a saturated aqueous sodium sulfite solution (100 mL)
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate)

出典と根拠

ORDレコード
ord-ce9aac6311a84498a2961369355d945b
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09169254B2

反応ノート

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