2-Chloroethanol → HCID 20716711, compound

HRID 1872305Notes

Reaction equation

HRID 1872305 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10]([O:12][CH3:13])=[O:11])=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].Cl[CH2:21][CH2:22][OH:23]>CN(C)C=O>[OH:23][CH2:22][CH2:21][O:1][C:2]1[CH:3]=[CH:4][C:5](/[CH:8]=[CH:9]/[C:10]([O:12][CH3:13])=[O:11])=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 342-ChloroethanolHCID 11430Potassium CarbonateHCID 92203Methyl p-coumarate

Product 1

HCID 20716711HCID 20716711, compoundYield 43.1%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

30 g (168 mmol) of methyl 3-(4-hydroxyphenyl)-acrylate (Example 1), 29 g (210 mmol) of anhydrous K2CO3 and a spatula tip of Kl were placed in 200 ml of dimethylformamide. 14.91 g (185 mmol) of 2-chloroethanol were added dropwise at 85° C. within 5 minutes while stirring. The batch was stirred at 85° C. for a further 3 days. Subsequently, the salts were filtered off and the filtrate was concentrated to dryness in a water-jet vacuum. 16.1 g of methyl (E)-3-[4-[2-hydroxyethoxy]-phenyl]-acrylate were obtained in the form of white crystals after recrystallization from i-propanol. ##STR17##

Workup

  1. stirringThe batch was stirred at 85° C. for a further 3 days
  2. filtrationSubsequently, the salts were filtered off
  3. concentrationthe filtrate was concentrated to dryness in a water-jet vacuum

Sources & evidence

ORD record
ord-fcfb366ed37f4564ad9c34fe7cc60f78
Source dataset
uspto-grants-2000_08
Patent number
US06107427

Reaction notes

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