Hydrochloric Acid → 3-(Hydroxymethyl)pyridin-2(1H)-one

HRID 85193Notes

Reaction equation

HRID 85193 reaction equation
C[Si](C)(C)[Si](C)(C)C.Cl[Si](C)(C)C.[OH:14][C:15]1[N:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17](O)=[O:18].[H-].C([Al+]CC(C)C)C(C)C.Cl>C1(C)C=CC=CC=1.ClCCl.CO>[OH:18][CH2:17][C:16]1[C:15](=[O:14])[NH:23][CH:22]=[CH:21][CH:20]=1

Participants

9

Conditions

Temperature
110 °C

Procedure

At RT, 23.2 g (144 mmol) of hexamethyldisilane and 0.781 g (7.19 mmol) of chlorotrimethylsilane are added to a suspension of 10.0 g (71.9 mmol) of 2-hydroxynicotinic acid in 100 ml of toluene, and the mixture is stirred with a KPG stirrer at 110° C. for 30 min. The mixture is then cooled to −40° C., and 22.5 g (158 mmol) of a 1 molar solution of diisobutylaluminium hydride in dichloromethane are added dropwise to the solution. The mixture is thawed to RT, stirred at RT for 18 h and finally, at −10° C., adjusted to pH=4 with dilute hydrochloric acid, and 500 ml of methanol are added such that the temperature does not exceed −10° C. The precipitate formed is filtered off, 100 ml of water are added to the filtrate, the mixture is stirred at 50° C. for 1 h and the precipitate is filtered off. Concentration of the filtrate gives 8.55 g (95% of theory) of the desired compound.

Workup

  1. temperatureThe mixture is then cooled to −40° C.
  2. customis thawed to RT
  3. stirringstirred at RT for 18 h
  4. customat −10° C.
  5. additionare added such that the temperature
  6. customdoes not exceed −10° C
  7. customThe precipitate formed
  8. filtrationis filtered off
  9. addition100 ml of water are added to the filtrate
  10. stirringthe mixture is stirred at 50° C. for 1 h
  11. filtrationthe precipitate is filtered off

Sources & evidence

ORD record
ord-01f0ea0c06b34f01bbb6314a5a902914
Source dataset
uspto-grants-2014_09
Patent number
US08846934B2

Reaction notes

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