Acetic Acid → HCID 10663825, compound

HRID 1608504Notes

Reaction equation

HRID 1608504 reaction equation
[C:1]1([NH:7][C:8]([C:10]2([CH3:27])[CH2:15][CH2:14][C:13]3[C:16]([CH3:26])=[C:17]([O:22]C(=O)C)[C:18]([CH3:21])=[C:19]([CH3:20])[C:12]=3[O:11]2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].C(O)(=O)C>C(O)C.O>[C:1]1([NH:7][C:8]([C:10]2([CH3:27])[CH2:15][CH2:14][C:13]3[C:16]([CH3:26])=[C:17]([OH:22])[C:18]([CH3:21])=[C:19]([CH3:20])[C:12]=3[O:11]2)=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Procedure

In a two-necked, round-bottomed flask, 2.75 g (7.48 mmol) of the compound obtained in Stage B of Example 1 are dissolved in 60 cm3 of 80% ethanol. Under a nitrogen stream, 18 cm3 of 2.5N sodium hydroxide are added. The mixture is left to stir at ordinary temperature for 2 h. The mixture is diluted with water, acidified with acetic acid and then the product is extracted with dichloromethane. The organic phase is washed with water and then dried. The mixture is purified by passing through a column of silica gel, eluting with isopropyl ether to obtain N-phenyl-6-hydroxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxamide (yield: 86%; melting point: 107°-109° C.) and then the reaction is carried out as in Stage C of Example 1, replacing N-phenyl-6-acetoxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxamide with N-phenyl-6-hydroxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxamide.

Workup

  1. waitThe mixture is left
  2. extractionthe product is extracted with dichloromethane
  3. washThe organic phase is washed with water
  4. customdried
  5. customThe mixture is purified
  6. washeluting with isopropyl ether

Sources & evidence

ORD record
ord-62ea2437ddac4f348e133d0b93dc6a0c
Source dataset
uspto-grants-1995_03
Patent number
US05395834

Reaction notes

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