Methanol → Methyl 3-(5-hydroxypyrimidin-2-yl)benzoate

HRID 1509845Notes

Reaction equation

HRID 1509845 reaction equation
[OH:1][C:2]1[CH:3]=[N:4][C:5]([C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([OH:13])=[O:12])=[N:6][CH:7]=1.S(Cl)(Cl)=O.[CH3:21]O>>[OH:1][C:2]1[CH:7]=[N:6][C:5]([C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([O:13][CH3:21])=[O:12])=[N:4][CH:3]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

78.8 g of 3-(5-hydroxypyrimidin-2-yl)benzoic acid are suspended in 1.4 l of absolute methanol, and 32.7 ml of thionyl chloride (449.8 mmol) are subsequently carefully added dropwise at RT. The reaction batch is warmed at 80° C. for 2 h. A further 20 ml of thionyl chloride (275.7 mmol) are added, and the mixture is warmed at 80° C. for a further 2 h. In order to complete the reaction, a further 10 ml of thionyl chloride (137.8 mmol) are added, and the mixture is warmed at 80° C. for a further 2 h. For work-up, 1000 ml of methanol are removed in a rotary evaporator, and the resultant residue is filtered off. The mother liquor is reduced to about 200 ml in the rotary evaporator, and the crystals formed are filtered off. The two crystal batches are combined, dried to constant weight at 50° C. in a vacuum drying cabinet.

Workup

  1. temperaturethe mixture is warmed at 80° C. for a further 2 h
  2. customthe reaction
  3. temperaturethe mixture is warmed at 80° C. for a further 2 h
  4. customFor work-up, 1000 ml of methanol are removed in a rotary evaporator
  5. filtrationthe resultant residue is filtered off
  6. customThe mother liquor is reduced to about 200 ml in the rotary evaporator
  7. customthe crystals formed
  8. filtrationare filtered off
  9. customdried to constant weight at 50° C. in a vacuum
  10. customdrying cabinet

Sources & evidence

ORD record
ord-672beea983f64bc5aced71fd6be02c4e
Source dataset
uspto-grants-2012_07
Patent number
US08211886B2

Reaction notes

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