Iodoethane → 3-Chloro-4-ethoxy-5-fluorobenzaldehyde

HRID 2038550Notes

Reaction equation

HRID 2038550 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([F:11])[C:9]=1[OH:10])[CH:5]=[O:6].[OH-].[K+].I[CH2:15][CH3:16]>C1COCC1.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([F:11])[C:9]=1[O:10][CH2:15][CH3:16])[CH:5]=[O:6]

Participants

6

Reactant 3

HCID 6340IodoethaneHCID 14797Potassium HydroxideHCID 27827873-Chloro-5-fluoro-4-hydroxybenzaldehyde

Product 1

HCID 201120653-Chloro-4-ethoxy-5-fluorobenzaldehydeYield 98%

Reagents, catalysts & solvents 2

HCID 962WaterSolvent2×HCID 8028TetrahydrofuranSolvent

Procedure

3-Chloro-5-fluoro-4-hydroxybenzaldehyde (1.0 gram, 5.7 mmol) in THF (40 mL) was heated at reflux for 17 hrs with KOH (534 mg, 9.5 mmol, 1.7 eq) in water (5 mL) and iodoethane (1 mL, 2.2 eq). The reaction was then transferred to a separatory funnel with water and extracted with methylene chloride (thrice, 150 mL each). The combined organic layers were washed with 10% aqueous HCl (40 mL), dried (MgSO4), and concentrated to a viscous orange liquid to yield 1.13 g of 3-chloro-4-ethoxy-5-fluorobenzaldehyde (98%). 1H-NMR (500 MHz, CDCl3): 9.84 (d, J=1.9 Hz, 1H), 7.71 (t, J=1.6 Hz, 1H), 7.53 (dd, J=1.9, 10.7 Hz, 1H), 4.37-4.32 (m, 2H), 1.47-1.40 (m, 3H).

Workup

  1. extractionextracted with methylene chloride (thrice, 150 mL each)
  2. washThe combined organic layers were washed with 10% aqueous HCl (40 mL)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated to a viscous orange liquid

Sources & evidence

ORD record
ord-e3494dd65292458589eaf8a171c7609d
Source dataset
uspto-grants-2013_11
Patent number
US08575208B2

Reaction notes

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