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Nitrogen → HCID 53689240, 화합물

HRID 1754994
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HRID 1754994 반응식
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]
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참가 물질

6

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

생성물 1

HCID 53689240HCID 53689240, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-ce9aac6311a84498a2961369355d945b
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169254B2

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