Sodium Iodide → Ethyl 4'-(3-iodopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate

HRID 253485Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 253485
[I-:1].[Na+].Br[CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:16][CH:15]=2)=[CH:10][C:9]=1[C:25]1[CH:34]=[CH:33][C:32]2[C:31]([CH3:36])([CH3:35])[CH2:30][CH2:29][C:28]([CH3:38])([CH3:37])[C:27]=2[CH:26]=1>CC(C)=O>[I:1][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:16][CH:15]=2)=[CH:10][C:9]=1[C:25]1[CH:34]=[CH:33][C:32]2[C:31]([CH3:36])([CH3:35])[CH2:30][CH2:29][C:28]([CH3:38])([CH3:37])[C:27]=2[CH:26]=1

Komponenten

4

Versuchsvorschrift

260 mg (1.73 mmol) of sodium iodide are added to a solution of 640 mg (1.16 mmol) of ethyl 4′-(3-bromopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate in 40 ml of acetone. The reaction mixture is stirred overnight at room temperature. The precipitate formed is filtered off and the filtrate is evaporated. 608 mg of ethyl 4′-(3-iodopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a white solid (m.p.=118° C., yield=71%).

Aufarbeitung

  1. customThe precipitate formed
  2. filtrationis filtered off
  3. customthe filtrate is evaporated

Quellen und Nachweise

ORD-Eintrag
ord-c3dd6a69042a4446b429a2e9d2b08250
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07872026B2

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