2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 54339148, compound

HRID 1109920Notes

Reaction equation

HRID 1109920 reaction equation
[CH3:1][CH:2]1[C@H:19]([C:20]([CH3:22])=[O:21])[C@:18]2([CH3:23])[C@H:4]([C@H:5]3[C@H:15]([CH2:16][CH2:17]2)[C@:14]2([CH3:24])[C:8](=[CH:9][C:10]([CH2:12][CH2:13]2)=[O:11])[CH2:7][CH2:6]3)[CH2:3]1.C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N>C1C=CC=CC=1>[CH3:1][C@@H:2]1[CH2:3][C@@H:4]2[C@:18]([CH3:23])([CH2:17][CH2:16][C@H:15]3[C@H:5]2[CH2:6][CH2:7][C:8]2[C@:14]3([CH3:24])[CH:13]=[CH:12][C:10](=[O:11])[CH:9]=2)[C@H:19]1[C:20](=[O:21])[CH3:22]

Participants

4

Procedure

A mixture of 16α-methylprogesterone (792 mg) , DDQ (575 mg) and benzene are heated at reflux for 28 hr, after 20 hr additional DDQ (70 mg) is added. After refluxing, the mixture is cooled to 20°-25°, filtered followed by basic workup (ether - potassium carbonate - magnesium sulfate) to give 16α-methylpregna-1,4-diene-3,20-dione.

Workup

  1. temperatureare heated
  2. additionis added
  3. temperatureAfter refluxing
  4. temperaturethe mixture is cooled to 20°-25°
  5. filtrationfiltered

Sources & evidence

ORD record
ord-02cd405092e2485fa75c517c27027ad8
Source dataset
uspto-grants-1994_06
Patent number
US05322943

Reaction notes

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