Pivalaldehyde → 2,2-Dimethyl-3-heptanol

HRID 39647Notes

Reaction equation

HRID 39647 reaction equation
[CH3:1][C:2]([CH:5]=[O:6])([CH3:4])[CH3:3].[Li][CH2:8][CH2:9][CH2:10][CH3:11]>C1COCC1.CCCCCC>[CH3:1][C:2]([CH3:4])([CH:5]([OH:6])[CH2:8][CH2:9][CH2:10][CH3:11])[CH3:3]

Participants

5

Conditions

Temperature
-65 °C

Procedure

20 g (0.232 mol) of pivaldehyde dissolved in 600 mL of THF was added to a 2 L 3-neck round bottom flask equipped with a magnetic stir bar, thermometer and rubber stopper. The vessel was maintained under N2. The reaction mixture was cooled to −65° C. in a dry ice/acetone bath. 112 mL (0.279 mmol) of a 2.5 M BuLi solution in hexane was slowly added in 5 mL portions with a 20 mL glass syringe, maintaining the temperature below −55° C. The reaction was stirred at −60° C. for one hour, then allowed to warm to −5° C. over one hour. The reaction was cooled again to −60° C. and slowly quenched with NH4Cl/H2O solution, maintaining the temperature below −50° C. 100 mL of water were added and the reaction was allowed to warm to room temperature. The THF was removed on a rotary evaporator with a bath temperature of 25° C. until an oil was observed. The product was extracted with ethyl ether, and the ether was dried and evaporated carefully to yield 31.0 g of 2,2-dimethyl-heptan-3-ol that was used directly in a subsequent oxidation reaction. 1H NMR (CDCl3, 500 MHz) δ (ppm): 3.2 (m, 1H), 1.2-1.7 (m, 3H), 0.93 (m, 3H), 0.89 (s, 9H).

Workup

  1. additionwas added to a 2 L 3-neck round bottom flask
  2. customequipped with a magnetic stir bar
  3. temperatureThe vessel was maintained under N2
  4. temperaturemaintaining the temperature below −55° C
  5. temperatureto warm to −5° C. over one hour
  6. temperatureThe reaction was cooled again to −60° C.
  7. customslowly quenched with NH4Cl/H2O solution
  8. temperaturemaintaining the temperature below −50° C
  9. addition100 mL of water were added
  10. temperatureto warm to room temperature
  11. customThe THF was removed on a rotary evaporator with a bath temperature of 25° C. until an oil
  12. extractionThe product was extracted with ethyl ether
  13. dry with materialthe ether was dried
  14. customevaporated carefully

Sources & evidence

ORD record
ord-9c6b7265041b4ca9b960f6ec0a328c40
Source dataset
uspto-grants-2013_09
Patent number
US08524948B2

Reaction notes

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