Dichlorodimethylsilane → HCID 10914335, compound

HRID 369514Notes

Reaction equation

HRID 369514 reaction equation
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].C1COCC1.[CH:11]1[CH2:12][CH:13]=[C:14]2[C:20]=1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2.[CH3:21][Si:22]([CH3:25])(Cl)Cl.[CH3:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>>[CH:3]1[CH:2]([Si:22]([CH:12]2[CH:11]=[C:20]3[C:14]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]3)=[CH:13]2)([CH3:25])[CH3:21])[CH:1]=[C:26]2[C:4]=1[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]2

Participants

6

Conditions

Temperature
-70 °C

Procedure

12 ml of a solution of n-butyllithium 2.5 M in hexane are added, at room temperature, to a solution in 100 ml of THF containing 4.1 grams (0.03 moles) of 2,4,5,6,7,8-hexahydroazulene (prepared as described in the copending patent application of the same applicant IT-A-MI 95A 002707). There is an exothermic reaction with the formation of a white solid. The mixture is left under stirring for 2 hours and is then cooled to -70° C. and 1.93 grams (0.015 moles) of dimethyldichlorosilane are added, over a period of about 20 minutes. The temperature is left to rise overnight and a yellow solution is finally obtained.

Workup

  1. customprepared
  2. customan exothermic reaction with the formation of a white solid
  3. waitThe mixture is left
  4. waitThe temperature is left
  5. waitto rise overnight
  6. customa yellow solution is finally obtained

Sources & evidence

ORD record
ord-776ab6df2ad3420aa59b6d97512038f0
Source dataset
uspto-grants-2000_10
Patent number
US06139484

Reaction notes

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