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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876862Generated: November 3, 2026

4-Nitroaniline → HCID 13450497, compound

https://huagongshe.com/reaction/1876862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitroanilineHCID 7475—
ReactantTetrahydrofuranHCID 8028—
ReactantCarbonochloridic acid, 3-chloropropyl esterHCID 69399—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 13450497HCID 1345049732.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-b31a4ba62eb74f43b20b0ce57877cc6f
Source noteuspto-grants-2012_11