HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 2,3-Dicyclohexyl-1-methyl-1-(3-(trimethoxysilyl)propyl)guanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Propanamine, N-methyl-3-(trimethoxysilyl)- | HCID 76480 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Product | 2,3-Dicyclohexyl-1-methyl-1-(3-(trimethoxysilyl)propyl)guanidine | HCID 58159261 | — |
Reaction Steps
A mixture of 23.23 g of N-methyl-(3-(trimethoxysilyl)propyl)amine (0.12 mol, 20% excess) and of 20.65 g of dicyclohexylcarbodiimide (0.1 mol) was heated for 6 h at 100° C. (carbodiimide conversion of 94%). The final colorless mixture was devolatilized at 100° C. under 2 mbar for 2 h to give 41.3 g of a colorless, moderately viscous liquid corresponding to the expected guanidine, containing 6% of the initial amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372935B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4751d33339d64701821659645dd72b63 |
| Source note | uspto-grants-2013_02 |