Ethoxyacetic acid → HCID 54707959, compound

HRID 2414440Notes

Reaction equation

HRID 2414440 reaction equation
[CH2:1]([O:3][CH2:4][C:5]([OH:7])=O)[CH3:2].[OH:8][C:9]1[C:14]2[CH:15]=[CH:16][C:17]([O:20][CH:21]3[CH2:26][CH2:25][CH2:24][CH2:23][O:22]3)=[C:18]([CH3:19])[C:13]=2[O:12][C:11](=[O:27])[CH:10]=1.Cl.CN(C)CCCN=C=NCC>ClCCl>[CH2:1]([O:3][CH2:4][C:5]([C:10]1[C:11](=[O:27])[O:12][C:13]2[C:18]([CH3:19])=[C:17]([O:20][CH:21]3[CH2:26][CH2:25][CH2:24][CH2:23][O:22]3)[CH:16]=[CH:15][C:14]=2[C:9]=1[OH:8])=[O:7])[CH3:2]

Participants

5

Procedure

2.21 ml of ethoxy acetic acid is added to a solution containing 5.00 g of 4-hydroxy-8-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2H-1-benzopyran-2-one, 7.30 g of 4-dimethyl-aminopyridine and 3.816 g of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride. This mixture is agitated for 16 hours at ambient temperature. After diluting with dichloromethane, washing is carried out with an aqueous solution of sodium dihydrogen phosphate then with brine. After drying over magnesium sulphate, filtering and evaporating to dryness, the product obtained is triturated in a hexane-ethyl acetate mixture (4-1). The product obtained is separated and dried. In this way 5.40 g of sought product is obtained.

Workup

  1. washwashing
  2. dry with materialAfter drying over magnesium sulphate
  3. filtrationfiltering
  4. customevaporating to dryness
  5. customthe product obtained
  6. customis triturated in a hexane-ethyl acetate mixture (4-1)
  7. customThe product obtained
  8. customis separated
  9. customdried

Sources & evidence

ORD record
ord-ae7854388949472ebf842abe67284599
Source dataset
uspto-grants-2004_11
Patent number
US06812331B2

Reaction notes

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