Diethyl Ether → HCID 12960838, compound

HRID 1075350Notes

Reaction equation

HRID 1075350 reaction equation
[Br-].[CH3:2][C:3]1[O:4][C:5]([CH3:28])=[C:6]([CH3:27])[C:7]=1[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH2:29]([Li])CCC.[F:34]/[C:35](=[C:41](\[CH:43]=O)/[CH3:42])/[C:36]([O:38][CH2:39][CH3:40])=[O:37].CCOCC>O1CCCC1.O>[F:34]/[C:35](=[C:41](/[CH3:42])\[CH:43]=[CH:29]\[C:7]1[C:6]([CH3:27])=[C:5]([CH3:28])[O:4][C:3]=1[CH3:2])/[C:36]([O:38][CH2:39][CH3:40])=[O:37]

Participants

7

Reactant 4

HCID 3283Diethyl EtherHCID 12960827HCID 12960827, compoundHCID 86736669HCID 86736669, compoundHCID 178418339Butyllithium

Product 1

HCID 12960838HCID 12960838, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-60 °C

Procedure

A suspension of 35 g.(75 mmol) of 2,4,5-trimethyl-3-furyl-triphenylphosphonium bromide in tetrahydrofuran was stirred under argon and cooled to -60° C. The ylide was formed by adding 1.1 equivalents of n-butyllithium and warming to -35° C. for 15 minutes. A solution of 10.6 g.(66 mmol) of ethyl 2Z-2-fluoro-3-formyl-butenoate in 50 ml. of ether was added slowly. After warming to 0° C., the reaction was poured into water and extracted with hexane. This was purified by partitioning between hexane and a 60% methanol/water solution. The hexane phase was washed with water, dried and partially evaporated. This solution containing ethyl 2Z,4E-2-fluoro-3-methyl-5-(2,4,5-trimethyl-3-furyl)pentadienoate was carried on to the next step without further purification.

Workup

  1. additionA suspension of 35 g
  2. customThe ylide was formed
  3. temperaturewarming to -35° C. for 15 minutes
  4. temperatureAfter warming to 0° C.
  5. extractionextracted with hexane
  6. customThis was purified
  7. customby partitioning between hexane
  8. washThe hexane phase was washed with water
  9. customdried
  10. custompartially evaporated
  11. additionThis solution containing ethyl 2Z,4E-2-fluoro-3-methyl-5-(2,4,5-trimethyl-3-furyl)pentadienoate
  12. customwas carried on to the next step without further purification

Sources & evidence

ORD record
ord-b4ee6b46bb994afbbcdafddaed43118b
Source dataset
uspto-grants-1983_07
Patent number
US04395575

Reaction notes

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