HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 10116033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 15521770 | HCID 15521770 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10116033 | HCID 10116033 | — |
Reaction Steps
0.26 ml of acetic acid, 0.14 ml of acetone and then 0.56 g of sodium triacetoxyborohydride are added to 0.40 g of the compound of Example 48 in 10 ml of 1,2-dichloroethane at room temperature. After stirring for 2 hours at room temperature, the reaction mixture is hydrolysed with an aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic phase is washed with water and dried over anhydrous sodium sulphate and the solvents are evaporated under reduced pressure. The expected product is obtained by filtration of the crystallized evaporation residue taken up in n-pentane;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673790B1 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-9c07f9b31b9f40aa99e4f90004a6c7ee |
| Source note | uspto-grants-2004_01 |