Nitrogen → Octanethioic acid, S-(3-(triethoxysilyl)propyl) ester
Reaction equation
N#N.[SH:3][CH2:4][CH2:5][CH2:6][Si:7]([O:14][CH2:15][CH3:16])([O:11][CH2:12][CH3:13])[O:8][CH2:9][CH3:10].C(N(CC)CC)C.[C:24](Cl)(=[O:32])[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>CCCCCC>[C:24]([S:3][CH2:4][CH2:5][CH2:6][Si:7]([O:14][CH2:15][CH3:16])([O:8][CH2:9][CH3:10])[O:11][CH2:12][CH3:13])(=[O:32])[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]Participants
Procedure
Into a 12-liter, three-necked round bottom flask equipped with mechanical stirrer, addition funnel, thermocouple, heating mantle, N2 inlet, and temperature controller were charged 1,021 grams of 3-mercaptopropyltriethoxysilane (SILQUEST® A-1891 silane from Crompton Corp.), 433 grams of triethylamine, and 3,000 mL of hexane. The solution was cooled in an ice bath, and 693 grams of octanoyl chloride were added over a two hour period via the addition funnel. After addition of the acid chloride was complete, the mixture was filtered two times, first through a 0.1 :m filter and then through a 0.01 :m filter, using a pressure filter to remove the salt. The solvent was removed under vacuum. The remaining yellow liquid was vacuum distilled to yield 1,349 grams of octanoylthiopropyltriethoxysilane as a clear, very light yellow liquid. The yield was 87 percent.
Workup
- customInto a 12-liter, three-necked round bottom flask equipped with mechanical stirrer, addition funnel
- temperatureThe solution was cooled in an ice bath
- filtrationthe mixture was filtered two times
- filtrationfirst through a 0.1 :m filter
- filtrationthrough a 0.01 :m filter
- filtrationfilter
- customto remove the salt
- customThe solvent was removed under vacuum
- distillationdistilled
Sources & evidence
- ORD record
- ord-cbc980fb19374796b86d3e7a7b21add3
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07432321B2
Reaction notes
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