2-(Dimethylamino)ethanol → HCID 70497649, compound

HRID 1424660Notes

Reaction equation

HRID 1424660 reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6](Cl)[N:5]=[C:4]([C:10]([O:12][CH3:13])=[O:11])[CH:3]=1.CN(C)[CH2:16][CH2:17]O.C([Zn]CC)C>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([CH2:16][CH3:17])[N:5]=[C:4]([C:10]([O:12][CH3:13])=[O:11])[CH:3]=1

Participants

6

Reactant 3

HCID 79022-(Dimethylamino)ethanolHCID 12993691Methyl 4,5,6-trichloropicolinateHCID 178418750HCID 178418750, compound

Product 1

HCID 70497649HCID 70497649, compound

Reagents, catalysts & solvents 2

HCID 178418476HCID 178418476, compoundCatalystHCID 8028TetrahydrofuranSolvent

Procedure

A 100 mL three-neck flask equipped with a reflux condenser and nitrogen inlet was charged with methyl 4,5,6-trichloropicolinate (2.40 g, 9.98 mmol). Anhydrous THF (50 mL) was added followed by N,N-dimethylethanolamine (0.20 g). The reaction mixture was sparged with nitrogen for 15 min Solid Pd(PPh3)2Cl2 (140 mg, 0.2 mmol) was added. The reaction mixture was stirred under nitrogen for 20 min Diethylzinc (1M solution in hexanes; 10 mL, 10 mmol) was added in 2 mL portions. When starting material was no longer observed through analysis by GC, the reaction mixture was quenched with water and extracted into EtOAc. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated under reduced pressure to a white solid (2.34 g). Analysis by GC-MS showed the solid contained 11% starting methyl 4,5,6-trichloropicolinate. 1H NMR (400 MHz, CDCl3) δ 8.06 (s, 1H, pyridine H), 4.01 (s, 3H, CO2Me), 3.10 (q, J=8 Hz, 2H, CH2), 1.33 (t, J=8 Hz, 3H, CH2CH3); 13C{1H} NMR (101 MHz, CDCl3) δ 164.4, 162.8, 145.4, 143.3, 132.9, 124.5 (C3), 53.1 (CO2Me), 30.0 (CH2), 12.3 (CH2CH3).

Workup

  1. customA 100 mL three-neck flask equipped with a reflux condenser and nitrogen inlet
  2. additionwas added
  3. additionwas added in 2 mL portions
  4. customthe reaction mixture was quenched with water
  5. extractionextracted into EtOAc
  6. washThe combined organic extracts were washed with brine
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated under reduced pressure to a white solid (2.34 g)

Sources & evidence

ORD record
ord-4f24b964484b47b9beee88c1aaf1ed2f
Source dataset
uspto-grants-2015_01
Patent number
US08927731B2

Reaction notes

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