HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86592830, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,3-diethoxyacetone | HCID 227346 | — |
| Reactant | HCID 178462451 | HCID 178462451 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86592830 | HCID 86592830 | 97.6% |
Reaction Steps
A solution (360 mL, 180 mmol) of ethynyl magnesium chloride in 0.5 M THF was stirred under ice-cooling and 1,3-diethoxyacetone (21.93 g, 150 mmol) was added dropwise. The mixture was stirred under ice-cooling for 30 min and acetic anhydride (18.4 mL, 195 mmol) was added dropwise. The mixture was stirred at room temperature for 1 hr. After the completion of the reaction, aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate and concentrated to give acetic acid 1,1-bis-ethoxymethyl-2-propynyl ester (31.36 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294629B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-21b0ac09a2d34e7eb9ca8e122e9c48fe |
| Source note | uspto-grants-2007_11 |