Dichlorodimethylsilane → HCID 66589487, compound
Reaction equation
[CH2:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH2:4][CH2:3][CH2:2]1.[CH2:14]([Li])[CH2:15][CH2:16][CH3:17].Cl[Si:20](Cl)([CH3:22])[CH3:21]>CCCCCC>[CH:10]1([Si:20]([CH:17]2[C:11]3[CH2:12][C:13]4[C:5](=[CH:4][CH:3]=[CH:2][CH:1]=4)[C:6]=3[CH2:14][CH2:15][CH2:16]2)([CH3:22])[CH3:21])[C:11]2[CH2:12][C:13]3[C:5](=[CH:4][CH:3]=[CH:2][CH:1]=3)[C:6]=2[CH2:7][CH2:8][CH2:9]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedure described in example 1 [step (c)], tetrahydrofluorene (17.6 mmol), butyllithium (11 ml of a solution 1.6M in hexane, 17.6 mmol) and dichlorodimethylsilane (1.07 ml, 8.81 mmol) gave a yellow oil.
Workup
- customgave a yellow oil
Sources & evidence
- ORD record
- ord-9f0ef7c4a59a4ae1b57f5ef1d6d90708
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06448424B1
Reaction notes
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