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Phenyl isocyanate → 5-Isoxazolemethanol, 3-dodecyl-

HRID 235164
Notes
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Reaction equation

HRID 235164 reaction equation
[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]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 241
Benzene
Solvent
2×

Conditions

Temperature
60 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-dff406c3167e48d0ae13c7c5ca7d8148
Source dataset
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05597838

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes