Reaction #7320

ord-3a033b9a8a09491ca1a0fe7d07fca5cf

Reaction equation

[K+].[OH-]
potassium hydroxide
Cl.NO
hydroxylamine hydrochloride
O=c1cc[nH]c(=O)[nH]1
uracil
C=O
paraformaldehyde
O=c1[nH]cc(CO)c(=O)[nH]1
5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione
Yield 14.5%

Solvents

Conditions

Temperature
51°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherreaction
  2. 2
    ConcentrationAfter concentration at 60° C./14 mmHg to a volume of ca. 500 mL
  3. 3
    workup.ADDITIONthe residue was diluted with acetone (500 mL)
  4. 4
    FiltrationThe resulting precipitate was collected by filtration
  5. 5
    Washwashed with acetone
  6. 6
    Otherdried by suction
  7. 7
    Otherat 50° C./25 mmHg to give crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (250 g) as a white solid
  8. 8
    ConcentrationThe combined mother liquor and washes were concentrated to a volume of ca. 100 mL
  9. 9
    FiltrationThe resulting precipitate was collected by filtration
  10. 10
    Washwashed with acetone
  11. 11
    Otherdried by suction

Procedure

A 2-L, three-necked flask equipped with a mechanical stirrer, thermometer, condenser, and nitrogen-inlet bubbler was charged with uracil (185.0 g, 1650 mmol) (Aldrich), paraformaldehyde (61.50 g, 2050 mmol as formaldehyde) (Aldrich), and a solution of potassium hydroxide (86.9%, 59.95 g, 928.5 mmol) (Aldrich) in water (1.445 L). The mixture was stirred at 50-52° C. for 68 h. TLC analysis indicated complete reaction. After concentration at 60° C./14 mmHg to a volume of ca. 500 mL, the residue was diluted with acetone (500 mL). The resulting precipitate was collected by filtration, washed with acetone, and dried by suction, then at 50° C./25 mmHg to give crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (250 g) as a white solid. The combined mother liquor and washes were concentrated to a volume of ca. 100 mL and a solution of hydroxylamine hydrochloride (27.52 g, 396.0 mmol, Aldrich) in water (100 mL) was added. The resulting precipitate was collected by filtration, washed with acetone, and dried by suction to give second crop of crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (34 g) as a white solid. The two lots were combined (244 g, 4% overweight) and used directly in the next step.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084270B2uspto-grants-2006_08