Hydrochloric Acid → HCID 14989019, compound

HRID 1904638Notes

Reaction equation

HRID 1904638 reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[CH2:5].C[O-].[Na+].[CH3:17][CH:18]([SH:20])[CH3:19].Cl>CO.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:13])[CH:4]([CH2:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1)[CH2:5][S:20][CH:18]([CH3:19])[CH3:17]

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 63642-PropanethiolHCID 575761Methyl 2-benzylprop-2-enoateHCID 10942334Sodium Methoxide

Product 1

HCID 14989019HCID 14989019, compound

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of methyl-2-benzylacrylate (20 gm, 0.113 mol) in methanol (100 ml) at room temperature was added a solution of sodium methoxide (2N, 17 ml) followed by isopropylthiol (12.56 ml). TLC (4:1, Hexanes: ethyl acetate) showed reaction to be complete after 30 min. The reaction mixture was made acidic with 1N HCl and extracted three times with ethyl acetate. The combined organic fractions were dried over NaSO4, filtered and evaporated in vacuo. The crude product was purified by chromatography (silica 4:1, hexanes: ethyl acetate to give methyl-3-isopropylthio-2-benzylpropionate.

Workup

  1. customreaction
  2. extractionextracted three times with ethyl acetate
  3. dry with materialThe combined organic fractions were dried over NaSO4
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customThe crude product was purified by chromatography (silica 4:1, hexanes

Sources & evidence

ORD record
ord-d56097db23d64ee3b446d986ec9fae33
Source dataset
uspto-grants-1989_06
Patent number
US04839357

Reaction notes

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