Acetic Acid → HCID 14726496, compound

HRID 1614096Notes

Reaction equation

HRID 1614096 reaction equation
C(O)(=O)C.[CH3:5][O:6][C:7]1[C:16]2[C:15]([CH3:18])([CH3:17])[CH2:14][CH2:13][C:12]([CH3:20])([CH3:19])[C:11]=2[CH:10]=[C:9]([C:21](Cl)=[O:22])[CH:8]=1.Br[CH2:25][C:26]1[CH:35]=[CH:34][C:29]([C:30]([O:32][CH3:33])=[O:31])=[CH:28][CH:27]=1>C(COC)OC.[Zn].C([O-])(=O)C.[Cu+2].C([O-])(=O)C.[Zn].[Cu].Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[C:30]([C:29]1[CH:34]=[CH:35][C:26]([CH2:25][C:21]([C:9]2[CH:8]=[C:7]([O:6][CH3:5])[C:16]3[C:15]([CH3:18])([CH3:17])[CH2:14][CH2:13][C:12]([CH3:20])([CH3:19])[C:11]=3[CH:10]=2)=[O:22])=[CH:27][CH:28]=1)([O:32][CH3:33])=[O:31]

Participants

9

Procedure

2.1 g of zinc powder and 0.21 g of copper(II) acetate were stirred with 7.3 ml of acetic acid at 20° C., with cooling, for 30 min. The zinc/copper couple was filtered off with suction and washed 2× with dry ether and 1× with dry dimethoxyethane. A solution of 4.5 g (16 mmol) of 5,6,7,8-tetrahydro-4-methoxy-5,5,8,8-tetramethylnaphthalene-2-carbonyl chloride and 3.7 g (16 mmol) of methyl 4-bromomethylbenzoate in 60 ml of dimethoxyethane was added dropwise to a suspension of the zinc/copper couple prepared in this way and of 0.56 g of bis(triphenylphosphine)palladium(II) chloride in 15 ml of dimethoxyethane at room temperature. The mixture was stirred for 75 min and then filtered through Celite, and the filtrate was concentrated. Three recrystallizations of the residue from methanol yielded 2.0 g of the title compound of melting point 143°-144° C.

Workup

  1. temperaturewith cooling, for 30 min
  2. filtrationThe zinc/copper couple was filtered off with suction
  3. washwashed 2× with dry ether and 1× with dry dimethoxyethane
  4. filtrationfiltered through Celite
  5. concentrationthe filtrate was concentrated
  6. customThree recrystallizations of the residue from methanol

Sources & evidence

ORD record
ord-f52893dfdbd647e4a958d00311f50961
Source dataset
uspto-grants-1993_03
Patent number
US05194664

Reaction notes

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