Ethylparaben → Ethyl4-(8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate

HRID 654225Notes

Reaction equation

HRID 654225 reaction equation
[CH3:1][C:2]1([CH3:15])[C:11]2[CH:10]=[C:9]([C:12]([OH:14])=[O:13])[CH:8]=[CH:7][C:6]=2[CH2:5][CH2:4][CH2:3]1.O[C:17]1[CH:27]=[CH:26][C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:19][CH:18]=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.C(Cl)Cl>[CH2:24]([O:23][C:21](=[O:22])[C:20]1[CH:26]=[CH:27][C:17]([O:13][C:12]([C:9]2[CH:8]=[CH:7][C:6]3[CH2:5][CH2:4][CH2:3][C:2]([CH3:15])([CH3:1])[C:11]=3[CH:10]=2)=[O:14])=[CH:18][CH:19]=1)[CH3:25]

Participants

6

Procedure

A solution of 220.7 mg (1.0804 mmol) of 8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoic acid, 180.6 mg (1.0868 mmol) of ethyl 4-hydroxybenzoate, 227.3 mg (1.1034 mmol) of 1,3-dicyclohexylcarbodiimide and 22.9 mg (0.1874 mmol) of 4-dimethylaminopyridine in 15 ml of methylene chloride was stirred at room temperature for 18 h. The reaction mixture was then filtered and the residue washed with 10 ml of methylene chloride. The filtrate was concentrated in-vacuo and the resultant crude product purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as a colorless oil.

Workup

  1. filtrationThe reaction mixture was then filtered
  2. washthe residue washed with 10 ml of methylene chloride
  3. concentrationThe filtrate was concentrated in-vacuo
  4. customthe resultant crude product purified by flash chromatography (silica; 5% ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-64d721e093af449da64921ce998ef16b
Source dataset
uspto-grants-1992_07
Patent number
US05130335

Reaction notes

Loading…