Phosphorus tribromide → HCID 22006938, compound

HRID 323826Notes

Reaction equation

HRID 323826 reaction equation
[CH2:1]([C:3]1[O:4][C:5]2[CH:11]=[CH:10][C:9]([CH2:12]O)=[CH:8][C:6]=2[N:7]=1)[CH3:2].P(Br)(Br)Br.C(N(CC)C(C)C)(C)C.[NH:27]1[CH2:32][CH2:31][CH:30]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:29][CH2:28]1>C1(C)C=CC=CC=1.O>[CH2:1]([C:3]1[O:4][C:5]2[CH:11]=[CH:10][C:9]([CH2:12][N:27]3[CH2:32][CH2:31][CH:30]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:29][CH2:28]3)=[CH:8][C:6]=2[N:7]=1)[CH3:2]

Participants

7

Reactant 4

HCID 24614Phosphorus tribromideHCID 70770Ethyl 4-piperidinecarboxylateHCID 81531DiisopropylethylamineHCID 22006939HCID 22006939, compound

Product 1

HCID 22006938HCID 22006938, compoundYield 34.9%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 1140TolueneSolvent2×

Procedure

To a stirred solution of 3.4 grams (0.019 mole) of (2-ethylbenzoxazol-5-yl)methanol in 25 mL of toluene was added 1.6 grams (0.006 mole) of phosphorous tribromide from a syringe. A precipitate formed immediately, and additional toluene was added to the reaction mixture to aid stirring. The reaction caused the reaction mixture temperature to rise to about 35° C. Upon completion of the addition, the reaction mixture stirred for an additional 20 minutes. The reaction mixture was then concentrated under reduced pressure to a residual solid. The solid was dissolved in 30 mL of dimethyl sulfoxide and, with stirring, 3.7 grams (0.029 mole) of N, N- diisopropylethylamine and 3.1 grams (0.019 mole) of ethyl piperidin-4-ylcarboxylate were added simultaneously from syringes. The resultant reaction caused the reaction mixture temperature to rise to about 40° C. The reaction mixture was allowed to cool to ambient temperature as it stirred for about 18 hours. The reaction mixture was poured into water and extracted with ethyl acetate and then with diethyl ether. The combined extracts were washed with an aqueous solution saturated with sodium bicarbonate, and then with an aqueous solution saturated with sodium chloride. The organic layer was concentrated under reduced pressure to a residual oil, which was subjected to column chromatography on silica gel, with ethyl acetate as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.1 grams of ethyl N-(2-ethylbenzoxazol-5-ylmethyl)piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

Workup

  1. customA precipitate formed immediately
  2. customto rise to about 35° C
  3. additionUpon completion of the addition
  4. stirringthe reaction mixture stirred for an additional 20 minutes
  5. concentrationThe reaction mixture was then concentrated under reduced pressure to a residual solid
  6. dissolutionThe solid was dissolved in 30 mL of dimethyl sulfoxide
  7. stirringwith stirring
  8. customThe resultant reaction
  9. customto rise to about 40° C
  10. stirringstirred for about 18 hours
  11. extractionextracted with ethyl acetate
  12. washThe combined extracts were washed with an aqueous solution saturated with sodium bicarbonate
  13. concentrationThe organic layer was concentrated under reduced pressure to a residual oil, which
  14. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-c1b59655b0764e2c8df5a4a79fc779a7
Source dataset
uspto-grants-2001_04
Patent number
US06214845B1

Reaction notes

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