Acetyl chloride → 3-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone

HRID 1834538Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1834538
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4](=[O:26])[C:5]([OH:25])=[C:6]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:7]2=[O:12].[O:27]1CC[CH2:29][CH2:28]1.[H-].[Na+].C(Cl)(=O)C>C(Cl)Cl>[C:28]([O:25][C:5]1[C:4](=[O:26])[C:3]2[C:8](=[CH:9][CH:10]=[CH:11][C:2]=2[Cl:1])[C:7](=[O:12])[C:6]=1[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])(=[O:27])[CH3:29]

Komponenten

6

Edukt 4

HCID 6367Acetyl chlorideHCID 8028Tetrahydrofuran4×HCID 24758Sodium hydrideHCID 178442826HCID 178442826, Verbindung

Produkt 1

HCID 213252433-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A solution of 0.95 parts of 5-chloro-2-dodecyl-3-hydroxy-1,4-naphthoquinone in 20 parts of anhydrous tetrahydrofuran was added under nitrogen to a mixture of 0.0635 parts of dispersed sodium hydride in 40 parts of tetrahydrofuran with stirring at room temperature. After 45 minutes of stirring, a solution of 0.275 parts of acetyl chloride in 30 parts of tetrahydrofuran was added and the mixture stirred for 5 hours. The tetrahydrofuran was stripped under reduced pressure and the residue taken up in methylene chloride and then washed with water, 10% hydrochloric acid, four more times with water, dried over sodium sulfate and stripped. The resulting yellow solid was purified by column chromatography on silica gel using 1-chlorobutane as eluent. Solvent removal gave 0.9 parts of 3-acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone, m.p. 57°-59° C.

Aufarbeitung

  1. stirringAfter 45 minutes of stirring
  2. stirringthe mixture stirred for 5 hours
  3. washwashed with water, 10% hydrochloric acid, four more times with water
  4. dry with materialdried over sodium sulfate
  5. customThe resulting yellow solid was purified by column chromatography on silica gel
  6. customSolvent removal

Quellen und Nachweise

ORD-Eintrag
ord-67b0bf36426741e48e159885ba850f98
Quelldatensatz
uspto-grants-1978_01
Patentnummer
US04070481

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