Ethanol → Ethyl 4-pentenoate

HRID 1901230Notes

Reaction equation

HRID 1901230 reaction equation
[C:1]([OH:7])(=[O:6])[CH2:2][CH2:3][CH:4]=[CH2:5].OS(O)(=O)=O.[CH2:13](O)[CH3:14]>C1C=CC=CC=1>[C:1]([O:7][CH2:13][CH3:14])(=[O:6])[CH2:2][CH2:3][CH:4]=[CH2:5]

Participants

5

Procedure

To a solution containing 4-pentenoic acid (20.73 g, 207 mmol) in ethanol (100 mL) and benzene (200 mL) was added H2SO4 (250 μL). The solution was refluxed and monitored by GC (50° C., 1 min to 250° C. at 10° C./min; DB-5; tR of acid 4.4 min, ester 3.8 min). After 15 h, the reaction was complete; about 1/2 of the solvent was removed under reduced pressure and diluted with 150 mL ether. This was extracted with H2O (1×150 mL), saturated NaHCO3 (2×150 mL), H2O(1×150 mL), and brine (1×100 mL). The organic layer was dried over K2CO3, the solvent was removed under water aspirator vacuum, and the residue was distilled to yield ethyl 4-pentenoate, a compound having the following structure: ##STR11## (20.79 g, 162 mmol, 78%; bp760 144° C.): 1H--NMR (200 MHc, CDCl3) δ 1.25 (t, J=7.2 Hz, 3 H, CH3), 2.36 (m, 4 H, CH2CH2), 4.14 (q, J=7.2 Hz, 2 H, OCH2), 4.95-5.13 (m, 2 H, H2C=), 5.81 (m, 1 H, =CH); 13C--NMR (50 MHc, CDCl3) δ 14.2 (CH3), 28.6, 33.5 (C--H2CH2), 115.3 (H2C=), 136.5 (=CH), 172.8 (C=O).

Workup

  1. temperatureThe solution was refluxed
  2. customabout 1/2 of the solvent was removed under reduced pressure
  3. additiondiluted with 150 mL ether
  4. extractionThis was extracted with H2O (1×150 mL), saturated NaHCO3 (2×150 mL), H2O(1×150 mL), and brine (1×100 mL)
  5. dry with materialThe organic layer was dried over K2CO3
  6. customthe solvent was removed under water
  7. distillationthe residue was distilled

Sources & evidence

ORD record
ord-0206f0e029d04fdc9cf735e302aba547
Source dataset
uspto-grants-1996_11
Patent number
US05576426

Reaction notes

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