Toluene → HCID 86600217, compound
Reaction equation
N[CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7].C1(C)C=CC=CC=1.[C:19](Cl)(=[O:21])[CH3:20].C([N:25](CC)CC)C>>[CH3:7][O:6][Si:5]([CH2:4][CH2:3][CH2:2][CH2:20][C:19]([NH2:25])=[O:21])([O:10][CH3:11])[O:8][CH3:9]Participants
5
Procedure
A three-neck round-bottomed flask, equipped with a mechanical stirrer, a refluxing condenser and a dropping funnel, was charged with 3-aminopropyltrimethoxysilane (18 gram, Gelest Inc.), toluene (40 mL, Aldrich) and triethylamine (13 gram, Aldrich). Stirring was started, and an appropriate acyl chloride such as acetyl chloride (18 mL, Aldrich) was added dropwise to the flask. The mixture was stirred at room temperature under an argon atmosphere for 16 hours.
Workup
- customA three-neck round-bottomed flask, equipped with a mechanical stirrer, a refluxing condenser and a dropping funnel
- stirringThe mixture was stirred at room temperature under an argon atmosphere for 16 hours
Sources & evidence
- ORD record
- ord-8a054f2e75814adfa1cc3ccec0d8df9f
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08702988B2
Reaction notes
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