Propanal → Ethyl 2-fluoro-3-hydroxypentanoate

HRID 576465Notes

Reaction equation

HRID 576465 reaction equation
[C:1]([O:4][CH2:5][CH:6](Br)[F:7])(=O)[CH3:2].[CH2:9]1C[O:12][CH2:11][CH2:10]1.C(OCC(Br)F)(=[O:16])C.C(=O)CC.C1COCC1.C(=O)CC.C(OC(C)C)(C)C>O>[F:7][CH:6]([CH:11]([OH:12])[CH2:10][CH3:9])[C:5]([O:4][CH2:1][CH3:2])=[O:16]

Participants

7

Procedure

After a 500 mL reaction vessel which had been sufficiently dried inside by vacuum heating was replaced with dry nitrogen, and placed in an ice bath, 24.2 g (370 mmol/1.5 equivalent) of activated metal zinc and 300 mL of THF (dehydrated) were added into the reaction vessel. Thereto was added a bromofluoroethyl acetate/THF solution (46.91 g (253.6 mmol/1.0 equivalent) of bromofluoroethyl acetate and 80 mL of THF (dehydrated)) dropwise over 5 min. After the dropwise addition, the temperature of the mixture was elevated to the room temperature, followed by stirring for 20 min. Thereto was added a propionaldehyde/THF solution (17.76 g (305.8 mmol/1.2 equivalent) of propionaldehyde and 80 mL of THF (dehydrated)), and the mixture was stirred for 60 min at a room temperature. Thereafter, water and diisopropyl ether were added thereto, and two-layer separation was carried out. The organic layer thus obtained was washed with diluted hydrochloric acid and water, and the moisture was eliminated using anhydrous magnesium sulfate, followed by filtration. Then diisopropyl ether was distilled off to give 35.4 g (yield: 85%) of ethyl 2-fluoro-3-hydroxy-pentanoate represented by the following formula.

Workup

  1. customAfter a 500 mL reaction vessel which
  2. customhad been sufficiently dried inside by vacuum
  3. temperatureheating
  4. customplaced in an ice bath
  5. addition24.2 g (370 mmol/1.5 equivalent) of activated metal zinc and 300 mL of THF (dehydrated) were added into the reaction vessel
  6. additionAfter the dropwise addition
  7. customwas elevated to the room temperature
  8. stirringthe mixture was stirred for 60 min at a room temperature
  9. customtwo-layer separation
  10. customThe organic layer thus obtained
  11. washwas washed with diluted hydrochloric acid and water
  12. filtrationfollowed by filtration
  13. distillationThen diisopropyl ether was distilled off

Sources & evidence

ORD record
ord-e4fb7c22f4fc468faafced8cd39319b3
Source dataset
uspto-grants-2015_05
Patent number
US09040221B2

Reaction notes

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