Hydrogen Peroxide → (2S)-2-(4-fluorophenyl)pent-4-enoic acid

HRID 1584487Notes

Reaction equation

HRID 1584487 reaction equation
C([C@H]1COC(=O)N1[C:14](=[O:26])[CH:15]([C:19]1[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=1)[CH2:16][CH:17]=[CH2:18])C1C=CC=CC=1.[O:27]1CCCC1.O.[OH-].[Li+].OO>[OH-].[Na+].O>[F:25][C:22]1[CH:21]=[CH:20][C:19]([C@H:15]([CH2:16][CH:17]=[CH2:18])[C:14]([OH:26])=[O:27])=[CH:24][CH:23]=1

Participants

7

Procedure

Combine (S)-4-benzyl-3-(2-(4-fluorophenyl)pent-4-enoyl)-2-oxazolidinone (9.66 g, 27.34 mol), tetrahydrofuran (160 mL), and water (40 mL). Cool in an ice bath. Add lithium hydroxide hydrate (2.52 g, 60 mmol) and an aqueous solution of hydrogen peroxide (10 mL, 30% 116 mmol). After 3 hours, dilute the reaction mixture with an aqueous 1 M sodium hydroxide solution and extract twice with diethyl ether. Cool the aqueous layer in an ice bath, acidify with an aqueous concentrated hydrochloric acid solution (about 15 mL), and extract twice with dichloromethane. Extract the combined organic layers with a saturated aqueous sodium thiosulfate solution, dry over MgSO4, filter, and evaporate in vacuo to give (S)-2-(4-fluorophenyl)pent-4-enoic acid.

Workup

  1. temperatureCool in an ice bath
  2. extractionextract twice with diethyl ether
  3. temperatureCool the aqueous layer in an ice bath
  4. extractionextract twice with dichloromethane
  5. extractionExtract the combined organic layers with a saturated aqueous sodium thiosulfate solution
  6. dry with materialdry over MgSO4
  7. filtrationfilter
  8. customevaporate in vacuo

Sources & evidence

ORD record
ord-0c599a3080fb4441b648822de3ef2628
Source dataset
uspto-grants-1999_08
Patent number
US05932571

Reaction notes

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