HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 67285454, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67284573 | HCID 67284573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67285454 | HCID 67285454 | 59.9% |
Reaction Steps
To a solution containing ethyl 3-(5-nitro-2-phenyl-1H-indol-1-yl) propan-1-ol (2.2 g; 7.4 mmol) and triethylamine (1.24 ml; 8.9 mmol) in CH2Cl2 (20 ml), acetyl chloride (0.6 ml; 8.9 mmol) was added dropwise; the reaction mixture was left under stirring at room temperature for 2 hours. Then water (20 ml) and NaHCO3 (saturated solution) were added to pH 7. The biphasic solution was transferred into a separating funnel extracted with CH2Cl2 (2×50 ml). The organic phases were combined, washed with brine (2×100 ml) and dried over Na2SO4. The solvent was removed by evaporation under reduced pressure to give 3-(5-nitro-2-phenyl-1H-indol-1-yl)propyl acetate (1.5 g), which was used without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871948B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-366c2b1d686a432bb2461209352c10db |
| Source note | uspto-grants-2014_10 |