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

HRID 2209895Notes

Reaction equation

HRID 2209895 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. additionis added
  2. temperatureAfter refluxing
  3. temperaturethe mixture is cooled to 20°-25°
  4. filtrationfiltered

Sources & evidence

ORD record
ord-ba7da3e3fd2e4815b905e9f3e4929a90
Source dataset
uspto-grants-1995_10
Patent number
USRE035053

Reaction notes

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