Hydrogen Peroxide → HCID 23437309, compound

HRID 2120024Notes

Reaction equation

HRID 2120024 reaction equation
[F:1][C:2]1(B(O)O)[CH:7]=[CH:6][C:5]([F:8])=[CH:4][CH:3]1[O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[OH:19]O.O>C1(C)C=CC=CC=1>[F:1][C:2]1[C:3]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])=[C:4]([OH:19])[C:5]([F:8])=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 784Hydrogen PeroxideHCID 962WaterHCID 69882765HCID 69882765, compound

Product 1

HCID 23437309HCID 23437309, compoundYield 87%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent2×

Procedure

White crystals of 1,4-difluoro-2-hexyloxybenzene-1-boronic acid (48 g) were dissolved in warm toluene (150 ml) and hydrogen peroxide (43 ml, 30%) was added drop-wise. Heating was continued for 45 min at 100° C. Once the solution had cooled to room temperature water was added (50 ml) and the layers were separated. The toluene layer was washed with ferrous ammonium sulphate (10%, 2×50 ml) and water (2×50 ml). The combined organic extracts were dried with magnesium sulphate, filtered and the solvent was removed to yield crude 3,6-difluoro,2-hexyloxyphenol as a pale yellow oil (31.67 g, 100%). The crude product was dissolved in toluene (150 ml), extracted with sodium hydroxide solution (10%w/v in methanol, 3×50 ml). The purple, aqueous extract, containing the phenoxide anion of the product, was then re-acidified with concentrated HCl until all of the colour had been displaced (pH˜4). The phenol was then extracted with dichloromethane (3×100 ml), washed with water (3×50 ml), dried with magnesium sulphate and filtered. Removal of the solvent in vacuo yielded the required product as an orange/brown oil (27.2 g, 87%). Kugelrohr distillation was performed under reduced pressure (2 mbar), the colourless distillate collected when the oven temp was 100° C. was found to contain only 4 (26.5 g, 82%), (Found: C, 62.65; H, 6.9. C12H16O2F2 requires C, 62.6; H, 6.9; O, 13.91; F, 16.52%); vmax(film)/cm−1 3524 and 2932 (C—H aliph), 2300 (C═C); δH(300 MHz; CDCl3) 0.90 (3H, t, 3J(H,H)=7 Hz, —CH3), 1.32 (4H, m, 2×—CH2—), 1.34 (2H, septet, 3J(H,H)=7 Hz, —CH2CH2CH2O—Ar), 1.76 (2H, quintet, 3J(H,H)=7 Hz, —CH2CH2CH2O—Ar), 4.17 (2H, t, 3J(H,H)=7 Hz, —CH2CH2O—Ar), 5.70 (1H, s, —OH, removed with D2O), 6.58 (1H, ddd, 3J(H,F)=13.3, 3J(H,H)=7.4, 4J(H,F)=4.5 Hz, C3H), 6.74 (1H, ddd, 3J(H,F)=18.3, 3J(H,H) 7.4, 4J(H,F)=4.6 Hz, C4H); δC(75 MHz 1H{BB}, INEPT; CDCl3) 14.31 (CH3), 22.91 (CH2), 25.78 (CH2), 30.34 (CH2), 31.87 (CH2), 74.90 (CH2), 106.65 (CH, dd, 2J(C,F)=15.1, 3J(C,F)=8.4 Hz, C4), 110.75 (CH, dd, 2J(C,F)=15.1, 3J(C,F)=8.4 Hz, C5), 135.67 (C, dd, 2J(C,F)=15.1, 3J(C,F)=8.4 Hz, C1), 138.42 (C, dd, 2J(C,F)=15.1, 3J(C,F)=8.4 Hz, C2), 147.65 (C, dd, 1J(C,F)=239, 4J(C,F)=2.6 Hz, C6), 151.7 (C, dd, 1J(C,F)=248, 4J(C,F)=2.6 Hz, C3); m/z 230 (M+, 10%), 146 (M+-alkoxy chain, 100%), 43 (50%).

Workup

  1. temperatureHeating
  2. additionwas added (50 ml)
  3. customthe layers were separated
  4. washThe toluene layer was washed with ferrous ammonium sulphate (10%, 2×50 ml) and water (2×50 ml)
  5. dry with materialThe combined organic extracts were dried with magnesium sulphate
  6. filtrationfiltered
  7. customthe solvent was removed
  8. customto yield crude 3,6-difluoro,2-hexyloxyphenol as a pale yellow oil (31.67 g, 100%)
  9. extractionextracted with sodium hydroxide solution (10%w/v in methanol, 3×50 ml)
  10. additionThe purple, aqueous extract, containing the phenoxide anion of the product
  11. extractionThe phenol was then extracted with dichloromethane (3×100 ml)
  12. washwashed with water (3×50 ml)
  13. dry with materialdried with magnesium sulphate
  14. filtrationfiltered
  15. customRemoval of the solvent in vacuo

Sources & evidence

ORD record
ord-5b6fd36ed19d4feb81c4c060d8a75c98
Source dataset
uspto-grants-2004_02
Patent number
US06689290B2

Reaction notes

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