HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-[5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 4-(2-Formyl-4-iodo-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 57743163 | — |
| Reactant | 5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-benzaldehyde | HCID 57743296 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 1-[5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene | HCID 66641536 | — |
Reaction Steps
In a manner similar to the method described in example 1d, 5-chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-benzaldehyde (1.5 g, 5 mmol) was used as the starting material in place of 4-(2-formyl-4-iodo-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester to react with 1,1,3,3,3-hexamethyldisilazane (0.8 g, 5 mmol), n-butyllithium (2.5 M, 2 mL, 5 mmol), trimethylsilyl chloride (0.55 g, 5 mmol), triethylamine (0.7 g, 6.8 mmol) and acetyl chloride (0.5 g, 6.8 mmol) to give crude 1-[5-chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-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 | US08134001B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-6d3b335b08c14016b052ccabd28f1b99 |
| Source note | uspto-grants-2012_03 |