Triethylamine → 2-(Isocyanomethyl)benzoxazole

HRID 1736667Notes

Reaction equation

HRID 1736667 reaction equation
[CH:1]([NH:3][CH2:4][C:5]1[O:6][C:7]2[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=2[N:9]=1)=O.C(N(CC)CC)C.P(Cl)(Cl)(Cl)=O.C(=O)([O-])[O-].[Na+].[Na+]>ClCCl.O>[N+:3]([CH2:4][C:5]1[O:6][C:7]2[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=2[N:9]=1)#[C-:1]

Participants

7

Procedure

To 2.83 g (16.1 mmol) of 2-(N-formylaminomethyl)benzoxazole, 7.39 ml (53.0 mmol) of triethylamine, and 30 ml of dichloromethane stirred at 0° are added dropwise 2.71 g (17.7 mmol) of phosphorous oxychloride in 5 ml of dichloromethane. The reaction mixture is stirred at 0° for 45 min and then 2.81 g of sodium carbonate dissolved in 20 ml of water is added. The mixture is stirred for 30 min and then partitioned between dichloromethane and aq. sodium bicarbonate. The organic layers are dried over sodium sulfate and concentrated and the crude product is chromatographed on silica gel (325 ml) eluting with ethyl acetate/hexane (10/90), the appropriate fractions are pooled and concentrated to give the title compound, mp 57.0°-57.5°; MS (m/z) 158; IR 766, 2166, 987, 1167 and 1230 cm-1 ; NMR (CDCl3) 4.94, 7.42, 7.58 and 7.76 δ.

Workup

  1. additionis added
  2. stirringThe mixture is stirred for 30 min
  3. custompartitioned between dichloromethane and aq. sodium bicarbonate
  4. dry with materialThe organic layers are dried over sodium sulfate
  5. concentrationconcentrated
  6. customthe crude product is chromatographed on silica gel (325 ml)
  7. washeluting with ethyl acetate/hexane (10/90)
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-dd13f622d17c4bb8909338002d4f3f63
Source dataset
uspto-grants-1996_07
Patent number
US05541324

Reaction notes

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