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Phenyl isocyanate → 5-Isoxazolemethanol, 3-dodecyl-

HRID 235164
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HRID 235164 반응식
[N+:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])([O-:3])=O.C[Si](C)(C)[O:19][C:20]#[C:21][CH3:22].C1(N=C=O)C=CC=CC=1.C(N(CC)CC)C>C1C=CC=CC=1>[CH2:5]([C:4]1[CH:22]=[C:21]([CH2:20][OH:19])[O:3][N:1]=1)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
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참가 물질

6

반응물 4

HCID 7672Phenyl isocyanateHCID 8471TriethylamineHCID 108233151-NitrotridecaneHCID 13614841O-trimethylsilylpropynol

생성물 1

HCID 106355535-Isoxazolemethanol, 3-dodecyl-수율 86%

시약·촉매·용매 1

HCID 241Benzene용매2회

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온도
60 °C

실험 절차

To a solution of 1-nitrotridecane (10.5 g) and O-trimethylsilyl-propynol (5.88 g) in dry benzene (100 ml) was added dropwise a solution of freshly distilled phenylisocyanate (10.9 g) and triethylamine (5.56 g) in dry benzene (40 ml) at 40° C., with mechanical stirring. The mixture was heated to 60° C. for 3.5 hr, cooled, and filtered. The filtrate was evaporated, taken up in tetrahydrofuran (300 ml) and 1.0M tetrabutylammonium fluoride (8 ml) was added. After 30 mins, the mixture was evaporated and the residue was purified by flash chromatography (silica gel, 2% methanol:dichloromethane). The appropriate fractions were collected and evaporated to give 10.5 g (86%) of product, mp 61°-63° C.

후처리

  1. temperaturecooled
  2. filtrationfiltered
  3. customThe filtrate was evaporated
  4. addition1.0M tetrabutylammonium fluoride (8 ml) was added
  5. customthe mixture was evaporated
  6. customthe residue was purified by flash chromatography (silica gel, 2% methanol:dichloromethane)
  7. customThe appropriate fractions were collected
  8. customevaporated

출처 및 근거

ORD 기록
ord-dff406c3167e48d0ae13c7c5ca7d8148
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05597838

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