Ammonium Chloride → HCID 86761087, compound
Reaction equation
C([Si]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11](/[C:15](/[CH2:19][CH3:20])=[CH:16]/[C:17]#[CH:18])[CH:10]=1)(C)C)(C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[Cl-].[NH4+]>C1COCC1>[CH2:19](/[C:15](/[C:11]1[CH:10]=[C:9]([OH:8])[CH:14]=[CH:13][CH:12]=1)=[CH:16]\[C:17]#[CH:18])[CH3:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1 g (3.5 mmol) of tert-butyl-[3-((E)-1-ethylbut-1-en-3-ynyl)phenoxy]dimethylsilane is dissolved in 50 ml of THF, and 3.8 ml (38 mmol) of a 1.0 M solution of tetrabutylammonium fluoride are added drop by drop. The mixture is stirred for 30 minutes, then treated with a saturated solution of ammonium chloride and extracted with ethyl acetate. A yellow oil is obtained (m=690 mg; Y=100%).
Workup
- extractionextracted with ethyl acetate
- customA yellow oil is obtained (m=690 mg; Y=100%)
Sources & evidence
- ORD record
- ord-0388b8b0163644c48977a31e787b087e
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700657B2
Reaction notes
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