HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitroaniline → HCID 13450497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Carbonochloridic acid, 3-chloropropyl ester | HCID 69399 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 13450497 | HCID 13450497 | 32.5% |
Reaction Steps
To a mixture of p-nitroaniline (0.50 g, 0.0036 mol) and 4-dimethylaminopyridine (DMAP, 0.531 g, 0.00434 mol) in tetrahydrofuran (10 mL, 0.1 mol) was added 3-chloropropyl chloridocarbonate (0.480 mL, 0.00398 mol). The mixture was stirred at room temperature for 1 h, then treated with 1.0 M of potassium tert-butoxide in tetrahydrofuran (7.96 mL, 0.00796 mol) at room temperature for 2 h, then quenched with aqueous ammonium chloride, extracted with EtOAc. The combined organic layers were washed with water, brine, dried and evaporated to dryness. The residue was purified on silica gel, eluting with 0 to 10% MeOH in dichloromethane, to provide the product (260 mg, 32.32%). LCMS (M+H) 222.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309718B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-b31a4ba62eb74f43b20b0ce57877cc6f |
| Source note | uspto-grants-2012_11 |