HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzhydrylamine → HCID 15113033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15113033 | HCID 15113033 | 30% |
Reaction Steps
A mixture of benzhydrylamine (25 g, 136.4 mmol) and trimethylsilylmethyl chloride (8.39 g, 68.4 mmol) in acetonitrile (105 ml) was refluxed overnight. Then the mixture was concentrated under vacuum at 70° C. with a rotary evaporator to remove all volatiles. The white residue was mixed with n-heptane (150 ml) and filtered over a glass filter. The salt residue was washed with n-heptane (2×25 ml). The combined heptane filtrates were concentrated under vacuum to give the crude product as a clear, slightly yellow oil (23 g; >100%). Purification by chromatography on silica gel (700 ml) eluting with n-heptane (2000 ml), followed by n-heptane:ethyl acetate (10:1) gave pure diphenyl-N-((trimethylsilyl)methyl)methanamine (5.5 g, 20.4 mmol; 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964739B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-2b34c23c52fa4ef38dde07cc3df49eb1 |
| Source note | uspto-grants-2011_06 |