Water → HCID 18787443, compound

HRID 1107546Notes

Reaction equation

HRID 1107546 reaction equation
[CH3:1][C:2]([CH2:4]Cl)=[CH2:3].[OH:6][C:7]1[CH:8]=[C:9]([CH:15]=[CH:16][CH:17]=1)[C:10]([O:12][CH2:13][CH3:14])=[O:11].C(=O)([O-])[O-].[K+].[K+].O>C1COCC1.CN(C=O)C>[CH2:13]([O:12][C:10](=[O:11])[C:9]1[CH:15]=[CH:16][CH:17]=[C:7]([O:6][CH:1]=[C:2]([CH3:4])[CH3:3])[CH:8]=1)[CH3:14]

Participants

7

Reactant 4

HCID 962WaterHCID 112413-Chloro-2-methyl-1-propeneHCID 11430Potassium CarbonateHCID 24522Ethyl 3-hydroxybenzoate

Product 1

HCID 18787443HCID 18787443, compound

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 8028TetrahydrofuranSolvent

Procedure

A mixture of 2-methyl-3-chloropropene (64.2 g, 710 mmol), ethyl 3-hydroxybenzoate (48.21 g, 590 mmol), and potassium carbonate (122.3 g, 890 mmol) in THF (600 ml) and DMF (600 ml) was heated to reflux for 6 hr. The mixure was poured into water (3 L) and extracted with ethyl acetate three times. The ethyl acetate extracts were combined and washed with water and dried with brine. The ethyl acetate extracts were concentrated in vacuo to a yellow oil that was vacuum distilled to a clear oil (112.9 g, 87%).

Workup

  1. temperaturewas heated
  2. temperatureto reflux for 6 hr
  3. extractionextracted with ethyl acetate three times
  4. washwashed with water
  5. dry with materialdried with brine
  6. concentrationThe ethyl acetate extracts were concentrated in vacuo to a yellow oil that
  7. distillationdistilled to a clear oil (112.9 g, 87%)

Sources & evidence

ORD record
ord-e5d25268025e45fb92a1c764f26299e5
Source dataset
uspto-grants-2000_05
Patent number
US06060506

Reaction notes

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