Pyridine → HCID 70408025, compound

HRID 2413862Notes

Reaction equation

HRID 2413862 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([C:9](=[O:16])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:3]=1.Cl.[C:18](Cl)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1.N1C=CC=CC=1>O>[C:18]([O:8][C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][C:4]=1[C:9](=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1

Participants

5

Reactant 3

HCID 1049PyridineHCID 6799Chlorohydroxy benzophenoneHCID 884383-Pyridinecarbonyl chloride, hydrochloride (1:1)

Product 1

HCID 70408025HCID 70408025, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
40 °C

Procedure

15 g (64.5 mmol) of p-chlorobenzoylphenol and 12 g (68 mmol) of nicotinic acid chloride hydrochloride was mixed with 200 ml dry pyridine and stirred for 24 hours at 40° C. After cooling 200 ml water were added and the precipitated product washed twice with 80 ml of water and recrystallized from methanol.

Workup

  1. additionwere added
  2. washthe precipitated product washed twice with 80 ml of water
  3. customrecrystallized from methanol

Sources & evidence

ORD record
ord-4c70fe3ffda3441e8ef267923006c6c7
Source dataset
uspto-grants-1988_01
Patent number
USRE032581

Reaction notes

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