HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 76568111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 1-Benzofuran-5-carbaldehyde | HCID 2773875 | — |
| Reactant | HCID 57565907 | HCID 57565907 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 76568111 | HCID 76568111 | — |
Reaction Steps
In a manner similar to the method described in example 190b, 1-benzofuran-5-carbaldehyde (1.2 g, 10 mmol) (Maybr-INT) was used as the starting material in place of 2-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-iodo-benzaldehyde to react with 1,1,3,3,3-hexamethyldisilazane (1.6 g, 10 mmol), n-butyllithium (2.5 M, 4 mL, 10 mmol), trimethylsilyl chloride (1.1 g, 10 mmol), triethylamine (1.36 g, 13.6 mmol) and acetyl chloride (1 g, 13.6 mmol) to give crude 1-(1-benzofuran-5-yl)-3-trimethylsilyoxy-2-aza-1,3-butadiene as a yellow gum and used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07495007B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-df9eede6dca24d7e8436d9c3eadedab4 |
| Source note | uspto-grants-2009_02 |