HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 131728679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 131728666 | HCID 131728666 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 131728679 | HCID 131728679 | — |
Reaction Steps
To a solution of compound of example 106 (3.35 g, 7.79 mmol) in dry CHCl3 (25 mL) was added acetic anhydride (1.76 g, 17.43 mmol) at 25° C. with stirring, followed by the addition of dimethylaminopyridine (0.033 g, 1% w/w). The mixture was stirred for 0.5 h. It was poured into ice water (50 mL), basified using a saturated aqueous Na2CO3 solution and extracted using CHCl3 (3×100 mL). The organic extract was washed with water, dried (anhydrous Na2SO4) and concentrated. The oil obtained was purified using a silica gel column and 0.1% MeOH+1% liquor NH3 in CHCl3 as eluant to get the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884127B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-779ac3a3d1bf412790d26605b3b43a7a |
| Source note | uspto-grants-2011_02 |