HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-(t-Butyldimethylsilyloxy)-1-hexyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol | HCID 11172555 | — |
| Reactant | Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester | HCID 86593935 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 6-(t-Butyldimethylsilyloxy)-1-hexyne | HCID 11009448 | — |
Reaction Steps
7-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol (27); and Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester (28, FIG. 4). A solution of 7-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol (27) (4.507 g, 21 mmol) in pyridine (20 mL) was treated with acetic anhydride (3.0 mL, 31.8 mmol). After 18 hours, the solvent was evaporated and the residue co-evaporated with toluene. The residue was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08900571B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-432f9a53badc436abf6d9ec10ad84d09 |
| Source note | uspto-grants-2014_12 |