Chlorodi(isopropyl)silane → HCID 123816274, compound
Reaction equation
[CH2:1]([SiH:5]([CH:9]([CH3:11])[CH3:10])[CH:6]([CH3:8])[CH3:7])[CH:2]([CH3:4])C.C([SiH](C(C)C)Cl)(C)C>>[CH:1]1([SiH:5]([CH:6]([CH3:7])[CH3:8])[CH:9]([CH3:10])[CH3:11])[CH2:2][CH2:4]1Participants
3
Procedure
The procedure of synthesizing Compound 40a was repeated, except that diisopropylchlorosilane (4.10 mL, 96.0 mmol) and cyclopropylmagnesium bromide THF solution (1.0M, 100 mL) were employed, whereby the Compound 44a was obtained as a colorless liquid (boiling point; 35 mmHg, 86 to 89° C. fraction, 1.84 g, 50%).
Sources & evidence
- ORD record
- ord-844775fd74eb46848986d4a150b8bd07
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825103B2
Reaction notes
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