HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → 2-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 2-Fluoro-5-iodobenzonitrile | HCID 2778928 | — |
| Product | 2-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrile | HCID 59305331 | — |
Reaction Steps
The title compound was prepared in substantially the same manner as described in Example 1, step 3 starting from 2-Fluoro-5-iodo-benzonitrile (1.0 g, 4.14 mmol), and Ethynyl-trimethyl-silane (0.487 g, 4.97 mmol), and was obtained as a waxy brown solid, (0.90 g, 99%), identified by NMR and mass spectral analyses. MS (EI+): 216 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723368B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-a1a427deb8c743a482ff039798a14629 |
| Source note | uspto-grants-2010_05 |