Potassium Hydroxide → (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid

HRID 1382513Notes

Reaction equation

HRID 1382513 reaction equation
C([O:3][C:4](=[O:27])[CH:5]([C:11]1([CH3:26])[CH2:16][CH2:15][C:14]2[C:17]([CH3:25])=[C:18]([O:23][CH3:24])[C:19]([CH3:22])=[C:20]([CH3:21])[C:13]=2[O:12]1)C(OCC)=O)C.[OH-].[K+]>C(O)CO.O>[CH3:24][O:23][C:18]1[C:19]([CH3:22])=[C:20]([CH3:21])[C:13]2[O:12][C:11]([CH3:26])([CH2:5][C:4]([OH:27])=[O:3])[CH2:16][CH2:15][C:14]=2[C:17]=1[CH3:25]

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 14210613rac-3,4-dihydro-2,5,7,8-tetramethyl-6-methoxy-2H-1-benzopyran-2-ylpropanedioic acid diethyl ester

Product 1

HCID 14210610(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acidYield 75.9%

Reagents, catalysts & solvents 1

HCID 20437942Ethylene glycol waterSolvent

Procedure

A mixture of 1.29 g (3.41 mmoles) of rac.-3,4-dihydro-2,5,7,8-tetramethyl-6-methoxy-2H-1-benzopyran-2-ylpropanedioic acid diethyl ester, 1.68 g of potassium hydroxide, and 75 ml of 9:1 parts by volume ethylene glycol-water mixture was stirred and refluxed for 6 hours. The resulting mixture was poured on ice and extracted with ether (the ether extract was discarded). The aqueous solution was acidified with 3N HCl and the precipitated acid was extracted 3 times with ether. The combined ether extracts were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. Purification of the residue by preparative thick layer chromatography gave 0.72 g (75.9%) of rac.-3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-acetic acid, as a colorless solid, mp 96°-98° C. Dimethylation using the procedure of example 14 gives rac.-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-acetic acid which can be converted to alpha-tocopherol as described in Helv. Chim. Acta. 59, 290 (1976).

Workup

  1. temperaturerefluxed for 6 hours
  2. additionThe resulting mixture was poured on ice
  3. extractionextracted with ether (the ether
  4. extractionextract
  5. extractionthe precipitated acid was extracted 3 times with ether
  6. washThe combined ether extracts were washed with brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customPurification of the residue by preparative thick layer chromatography

Sources & evidence

ORD record
ord-c7c98ed4910e415bba94309a72ee104a
Source dataset
uspto-grants-1989_02
Patent number
US04806661

Reaction notes

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