HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879906Generated: October 29, 2026
Hydrochloric Acid → HCID 123297189, compound
https://huagongshe.com/reaction/879906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dichlorosilane | HCID 61330 | — |
| Reactant | Nanofin | HCID 68843 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 123297189 | HCID 123297189 | 66% |
Reaction Steps
In a 2000 ml 3-necked round bottom flask equipped with mechanical stirror and an addition funnel, 1000 ml hexane was added. With the flask was cooled to −20° C. using a dry ice IPA cold bath, 101 g (1.0 mol) dichlorosilane was condensed and dissolved into hexane. With stirring, a mixture of 113 g (1.0 mol) 2,6-dimethylpiperidine and 111 g (1.1 mol) triethylamine was added dropwise to the flask. After the addition was complete, the reaction mixture was stirred at −20° C. for 1 hour, and then let warming up to room temperature. A salt byproduct precipitate of HCl.Et3N was removed by vacuum filtration in a glove bag purging with N2 to prevent the product reacting with the moisture in the air. A GC/MS analysis on the filtrate confirmed the product 2,6-dimethylpiperidinochlorosilane, showing the product with a molecular ion mass of 177 and supporting mass fragment of mass M —CH3 of 162. The solvent hexane was removed by distillation and the product was separated by vacuum distillation. The boiling point was 60° C. at 10 torr. The yield was 66%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993072B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-75996917812e44469c9f9c83d4c2d4dc |
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| Source note | uspto-grants-2015_03 |
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