HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → Bis(t-butylamino)silacyclobutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 1,1-Dichlorosilacyclobutane | HCID 75373 | — |
| Product | Bis(t-butylamino)silacyclobutane | HCID 12029860 | 45% |
Reaction Steps
Bis(t-butylamino)silacyclobutane (BTBSCB) was synthesized by reacting 1,1-dichlorosilacyclobutane with an excess amount of t-butylamine (Equation 1). To do so, 19.7 ml (0.166 mol) 1,1-dichlorosilacyclobutane was added to 105 ml (0.999 mol) t-butylamine in 1 L hexanes at 0° C. After bodying for three days at the room temperature, the reaction slurry was filtered to remove t-butylamine hydrochloride salt. The filtrant was vacuum dried to give a crude liquid product which was then vacuum distilled. 16 g Product was isolated at 99.2% purity in 45% yield at 71° C. under 50 torr pressure. The structure of the product analyzed with 1H, 13C and 29Si NMR, FT-IR and GC-MS was in consistence with bis(t-butylamino)silacyclobutane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09117664B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-56a8efb2fd2440c89f6c0eaffe2e1bd8 |
| Source note | uspto-grants-2015_08 |